Canonical Allele Identifier: CA369588833
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781581C>A , CM000669.2:g.140781581C>A GRCh38
NC_000007.13:g.140481381C>A , CM000669.1:g.140481381C>A GRCh37
NC_000007.12:g.140127850C>A NCBI36
NG_007873.3:g.148184G>T , LRG_299:g.148184G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1427G>T MANE Select ENSP00000493543.1:p.Trp476Leu
ENST00000288602.11:c.1547G>T ENSP00000288602.7:p.Trp516Leu
ENST00000479537.6:c.97G>T
ENST00000496384.7:c.1427G>T ENSP00000419060.2:p.Trp476Leu
ENST00000497784.2:c.*877G>T ENSP00000420119.2:n.*877G>T
ENST00000642228.1:c.*505G>T ENSP00000493678.1:n.*505G>T
ENST00000642875.1:n.869G>T
ENST00000644120.1:n.1817G>T
ENST00000644650.1:c.523G>T
ENST00000644905.1:n.1516G>T
ENST00000644969.2:c.1547G>T MANE Plus Clinical ENSP00000496776.1:p.Trp516Leu
ENST00000646334.1:n.557G>T
ENST00000646730.1:c.1427G>T ENSP00000494784.1:p.Trp476Leu
ENST00000646891.1:c.1427G>T ENSP00000493543.1:p.Trp476Leu
ENST00000647434.1:c.470G>T ENSP00000495132.1:p.Trp157Leu
ENST00000288602.10:c.1427G>T ENSP00000288602.6:p.Trp476Leu
ENST00000496384.6:c.250G>T
ENST00000497784.1:c.1462G>T ENSP00000420119.1:n.1462G>T
NM_004333.4:c.1427G>T , LRG_299t1:c.1427G>T NP_004324.2:p.Trp476Leu
XM_005250045.1:c.1427G>T XP_005250102.1:p.Trp476Leu
XM_005250046.1:c.1427G>T XP_005250103.1:p.Trp476Leu
XM_011516529.1:c.1427G>T XP_011514831.1:p.Trp476Leu
XM_011516530.1:c.1427G>T XP_011514832.1:p.Trp476Leu
XR_242190.1:n.1435G>T
XR_927520.1:n.1435G>T
XR_927521.1:n.1435G>T
XR_927522.1:n.1435G>T
XR_927523.1:n.1435G>T
NM_001354609.1:c.1427G>T NP_001341538.1:p.Trp476Leu
NM_004333.5:c.1427G>T NP_004324.2:p.Trp476Leu
NR_148928.1:n.1732G>T
XM_017012558.1:c.1547G>T XP_016868047.1:p.Trp516Leu
XM_017012559.1:c.1547G>T XP_016868048.1:p.Trp516Leu
XR_001744857.1:n.1555G>T
XR_001744858.1:n.1555G>T
NM_001354609.2:c.1427G>T NP_001341538.1:p.Trp476Leu
NM_001374244.1:c.1547G>T NP_001361173.1:p.Trp516Leu
NM_001374258.1:c.1547G>T MANE Plus Clinical NP_001361187.1:p.Trp516Leu
NM_004333.6:c.1427G>T MANE Select NP_004324.2:p.Trp476Leu
NM_001378467.1:c.1436G>T NP_001365396.1:p.Trp479Leu
NM_001378468.1:c.1427G>T NP_001365397.1:p.Trp476Leu
NM_001378469.1:c.1361G>T NP_001365398.1:p.Trp454Leu
NM_001378470.1:c.1325G>T NP_001365399.1:p.Trp442Leu
NM_001378471.1:c.1316G>T NP_001365400.1:p.Trp439Leu
NM_001378472.1:c.1271G>T NP_001365401.1:p.Trp424Leu
NM_001378473.1:c.1271G>T NP_001365402.1:p.Trp424Leu
NM_001378474.1:c.1427G>T NP_001365403.1:p.Trp476Leu
NM_001378475.1:c.1163G>T NP_001365404.1:p.Trp388Leu