Canonical Allele Identifier: CA458115920
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2129023498
MyVariant Identifiers: chr7:g.140481389C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781589C>T , CM000669.2:g.140781589C>T GRCh38
NC_000007.13:g.140481389C>T , CM000669.1:g.140481389C>T GRCh37
NC_000007.12:g.140127858C>T NCBI36
NG_007873.3:g.148176G>A , LRG_299:g.148176G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1419G>A MANE Select ENSP00000493543.1:p.Lys473=
ENST00000288602.11:c.1539G>A ENSP00000288602.7:p.Lys513=
ENST00000479537.6:c.89G>A
ENST00000496384.7:c.1419G>A ENSP00000419060.2:p.Lys473=
ENST00000497784.2:c.*869G>A ENSP00000420119.2:n.*869G>A
ENST00000642228.1:c.*497G>A ENSP00000493678.1:n.*497G>A
ENST00000642875.1:n.861G>A
ENST00000644120.1:n.1809G>A
ENST00000644650.1:c.515G>A
ENST00000644905.1:n.1508G>A
ENST00000644969.2:c.1539G>A MANE Plus Clinical ENSP00000496776.1:p.Lys513=
ENST00000646334.1:n.549G>A
ENST00000646730.1:c.1419G>A ENSP00000494784.1:p.Lys473=
ENST00000646891.1:c.1419G>A ENSP00000493543.1:p.Lys473=
ENST00000647434.1:c.462G>A ENSP00000495132.1:p.Lys154=
ENST00000288602.10:c.1419G>A ENSP00000288602.6:p.Lys473=
ENST00000496384.6:c.242G>A
ENST00000497784.1:c.1454G>A ENSP00000420119.1:n.1454G>A
NM_004333.4:c.1419G>A , LRG_299t1:c.1419G>A NP_004324.2:p.Lys473=
XM_005250045.1:c.1419G>A XP_005250102.1:p.Lys473=
XM_005250046.1:c.1419G>A XP_005250103.1:p.Lys473=
XM_011516529.1:c.1419G>A XP_011514831.1:p.Lys473=
XM_011516530.1:c.1419G>A XP_011514832.1:p.Lys473=
XR_242190.1:n.1427G>A
XR_927520.1:n.1427G>A
XR_927521.1:n.1427G>A
XR_927522.1:n.1427G>A
XR_927523.1:n.1427G>A
NM_001354609.1:c.1419G>A NP_001341538.1:p.Lys473=
NM_004333.5:c.1419G>A NP_004324.2:p.Lys473=
NR_148928.1:n.1724G>A
XM_017012558.1:c.1539G>A XP_016868047.1:p.Lys513=
XM_017012559.1:c.1539G>A XP_016868048.1:p.Lys513=
XR_001744857.1:n.1547G>A
XR_001744858.1:n.1547G>A
NM_001354609.2:c.1419G>A NP_001341538.1:p.Lys473=
NM_001374244.1:c.1539G>A NP_001361173.1:p.Lys513=
NM_001374258.1:c.1539G>A MANE Plus Clinical NP_001361187.1:p.Lys513=
NM_004333.6:c.1419G>A MANE Select NP_004324.2:p.Lys473=
NM_001378467.1:c.1428G>A NP_001365396.1:p.Lys476=
NM_001378468.1:c.1419G>A NP_001365397.1:p.Lys473=
NM_001378469.1:c.1353G>A NP_001365398.1:p.Lys451=
NM_001378470.1:c.1317G>A NP_001365399.1:p.Lys439=
NM_001378471.1:c.1308G>A NP_001365400.1:p.Lys436=
NM_001378472.1:c.1263G>A NP_001365401.1:p.Lys421=
NM_001378473.1:c.1263G>A NP_001365402.1:p.Lys421=
NM_001378474.1:c.1419G>A NP_001365403.1:p.Lys473=
NM_001378475.1:c.1155G>A NP_001365404.1:p.Lys385=