Canonical Allele Identifier: CA2695208553
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781605_140781613del , CM000669.2:g.140781605_140781613del GRCh38
NC_000007.13:g.140481405_140481413del , CM000669.1:g.140481405_140481413del GRCh37
NC_000007.12:g.140127874_140127882del NCBI36
NG_007873.3:g.148156_148164del , LRG_299:g.148156_148164del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1399_1407del MANE Select ENSP00000493543.1:p.Ser467_Gly469del
ENST00000288602.11:c.1519_1527del ENSP00000288602.7:p.Ser507_Gly509del
ENST00000479537.6:c.69_77del
ENST00000496384.7:c.1399_1407del ENSP00000419060.2:p.Ser467_Gly469del
ENST00000497784.2:c.*849_*857del ENSP00000420119.2:n.*849_*857del
ENST00000642228.1:c.*477_*485del ENSP00000493678.1:n.*477_*485del
ENST00000642875.1:n.841_849del
ENST00000644120.1:n.1789_1797del
ENST00000644650.1:c.495_503del
ENST00000644905.1:n.1488_1496del
ENST00000644969.2:c.1519_1527del MANE Plus Clinical ENSP00000496776.1:p.Ser507_Gly509del
ENST00000646334.1:n.529_537del
ENST00000646730.1:c.1399_1407del ENSP00000494784.1:p.Ser467_Gly469del
ENST00000646891.1:c.1399_1407del ENSP00000493543.1:p.Ser467_Gly469del
ENST00000647434.1:c.442_450del ENSP00000495132.1:p.Ser148_Gly150del
ENST00000288602.10:c.1399_1407del ENSP00000288602.6:p.Ser467_Gly469del
ENST00000496384.6:c.222_230del
ENST00000497784.1:c.1434_1442del ENSP00000420119.1:n.1434_1442del
NM_004333.4:c.1399_1407del , LRG_299t1:c.1399_1407del NP_004324.2:p.Ser467_Gly469del
XM_005250045.1:c.1399_1407del XP_005250102.1:p.Ser467_Gly469del
XM_005250046.1:c.1399_1407del XP_005250103.1:p.Ser467_Gly469del
XM_011516529.1:c.1399_1407del XP_011514831.1:p.Ser467_Gly469del
XM_011516530.1:c.1399_1407del XP_011514832.1:p.Ser467_Gly469del
XR_242190.1:n.1407_1415del
XR_927520.1:n.1407_1415del
XR_927521.1:n.1407_1415del
XR_927522.1:n.1407_1415del
XR_927523.1:n.1407_1415del
NM_001354609.1:c.1399_1407del NP_001341538.1:p.Ser467_Gly469del
NM_004333.5:c.1399_1407del NP_004324.2:p.Ser467_Gly469del
NR_148928.1:n.1704_1712del
XM_017012558.1:c.1519_1527del XP_016868047.1:p.Ser507_Gly509del
XM_017012559.1:c.1519_1527del XP_016868048.1:p.Ser507_Gly509del
XR_001744857.1:n.1527_1535del
XR_001744858.1:n.1527_1535del
NM_001354609.2:c.1399_1407del NP_001341538.1:p.Ser467_Gly469del
NM_001374244.1:c.1519_1527del NP_001361173.1:p.Ser507_Gly509del
NM_001374258.1:c.1519_1527del MANE Plus Clinical NP_001361187.1:p.Ser507_Gly509del
NM_004333.6:c.1399_1407del MANE Select NP_004324.2:p.Ser467_Gly469del
NM_001378467.1:c.1408_1416del NP_001365396.1:p.Ser470_Gly472del
NM_001378468.1:c.1399_1407del NP_001365397.1:p.Ser467_Gly469del
NM_001378469.1:c.1333_1341del NP_001365398.1:p.Ser445_Gly447del
NM_001378470.1:c.1297_1305del NP_001365399.1:p.Ser433_Gly435del
NM_001378471.1:c.1288_1296del NP_001365400.1:p.Ser430_Gly432del
NM_001378472.1:c.1243_1251del NP_001365401.1:p.Ser415_Gly417del
NM_001378473.1:c.1243_1251del NP_001365402.1:p.Ser415_Gly417del
NM_001378474.1:c.1399_1407del NP_001365403.1:p.Ser467_Gly469del
NM_001378475.1:c.1135_1143del NP_001365404.1:p.Ser379_Gly381del