Canonical Allele Identifier: CA458115941

Gene: BRAF

Linked Data

• dbSNP Id: rs1428310180
• gnomAD v3: 7-140781619-A-T
• gnomAD v4: 7-140781619-A-T
• MyVariant Identifiers: chr7:g.140481419A>T (hg19) ; chr7:g.140781619A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781619A>T , CM000669.2:g.140781619A>T	GRCh38
NC_000007.13:g.140481419A>T , CM000669.1:g.140481419A>T	GRCh37
NC_000007.12:g.140127888A>T	NCBI36
NG_007873.3:g.148146T>A , LRG_299:g.148146T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1389T>A MANE Select	ENSP00000493543.1:p.Ile463=
ENST00000288602.11:c.1509T>A	ENSP00000288602.7:p.Ile503=
ENST00000479537.6:c.59T>A
ENST00000496384.7:c.1389T>A	ENSP00000419060.2:p.Ile463=
ENST00000497784.2:c.*839T>A	ENSP00000420119.2:n.*839T>A
ENST00000642228.1:c.*467T>A	ENSP00000493678.1:n.*467T>A
ENST00000642875.1:n.831T>A
ENST00000644120.1:n.1779T>A
ENST00000644650.1:c.485T>A
ENST00000644905.1:n.1478T>A
ENST00000644969.2:c.1509T>A MANE Plus Clinical	ENSP00000496776.1:p.Ile503=
ENST00000646334.1:n.519T>A
ENST00000646730.1:c.1389T>A	ENSP00000494784.1:p.Ile463=
ENST00000646891.1:c.1389T>A	ENSP00000493543.1:p.Ile463=
ENST00000647434.1:c.432T>A	ENSP00000495132.1:p.Ile144=
ENST00000288602.10:c.1389T>A	ENSP00000288602.6:p.Ile463=
ENST00000496384.6:c.212T>A
ENST00000497784.1:c.1424T>A	ENSP00000420119.1:n.1424T>A
NM_004333.4:c.1389T>A , LRG_299t1:c.1389T>A	NP_004324.2:p.Ile463=
XM_005250045.1:c.1389T>A	XP_005250102.1:p.Ile463=
XM_005250046.1:c.1389T>A	XP_005250103.1:p.Ile463=
XM_011516529.1:c.1389T>A	XP_011514831.1:p.Ile463=
XM_011516530.1:c.1389T>A	XP_011514832.1:p.Ile463=
XR_242190.1:n.1397T>A
XR_927520.1:n.1397T>A
XR_927521.1:n.1397T>A
XR_927522.1:n.1397T>A
XR_927523.1:n.1397T>A
NM_001354609.1:c.1389T>A	NP_001341538.1:p.Ile463=
NM_004333.5:c.1389T>A	NP_004324.2:p.Ile463=
NR_148928.1:n.1694T>A
XM_017012558.1:c.1509T>A	XP_016868047.1:p.Ile503=
XM_017012559.1:c.1509T>A	XP_016868048.1:p.Ile503=
XR_001744857.1:n.1517T>A
XR_001744858.1:n.1517T>A
NM_001354609.2:c.1389T>A	NP_001341538.1:p.Ile463=
NM_001374244.1:c.1509T>A	NP_001361173.1:p.Ile503=
NM_001374258.1:c.1509T>A MANE Plus Clinical	NP_001361187.1:p.Ile503=
NM_004333.6:c.1389T>A MANE Select	NP_004324.2:p.Ile463=
NM_001378467.1:c.1398T>A	NP_001365396.1:p.Ile466=
NM_001378468.1:c.1389T>A	NP_001365397.1:p.Ile463=
NM_001378469.1:c.1323T>A	NP_001365398.1:p.Ile441=
NM_001378470.1:c.1287T>A	NP_001365399.1:p.Ile429=
NM_001378471.1:c.1278T>A	NP_001365400.1:p.Ile426=
NM_001378472.1:c.1233T>A	NP_001365401.1:p.Ile411=
NM_001378473.1:c.1233T>A	NP_001365402.1:p.Ile411=
NM_001378474.1:c.1389T>A	NP_001365403.1:p.Ile463=
NM_001378475.1:c.1125T>A	NP_001365404.1:p.Ile375=