Canonical Allele Identifier: CA457985912

Gene: BRAF

Linked Data

• dbSNP Id: rs1205982094
• gnomAD v3: 7-140749377-G-A
• gnomAD v4: 7-140749377-G-A
• MyVariant Identifiers: chr7:g.140449177G>A (hg19) ; chr7:g.140749377G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749377G>A , CM000669.2:g.140749377G>A	GRCh38
NC_000007.13:g.140449177G>A , CM000669.1:g.140449177G>A	GRCh37
NC_000007.12:g.140095646G>A	NCBI36
NG_007873.3:g.180388C>T , LRG_299:g.180388C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1902C>T MANE Select	ENSP00000493543.1:p.Ser634=
ENST00000288602.11:c.2022C>T	ENSP00000288602.7:p.Ser674=
ENST00000479537.6:c.572C>T
ENST00000496384.7:c.1902C>T	ENSP00000419060.2:p.Ser634=
ENST00000497784.2:c.*1352C>T	ENSP00000420119.2:n.*1352C>T
ENST00000642228.1:c.*980C>T	ENSP00000493678.1:n.*980C>T
ENST00000642875.1:n.1300C>T
ENST00000644120.1:n.2292C>T
ENST00000644650.1:c.998C>T
ENST00000644905.1:n.2784C>T
ENST00000644969.2:c.2022C>T MANE Plus Clinical	ENSP00000496776.1:p.Ser674=
ENST00000646730.1:c.*478C>T	ENSP00000494784.1:n.*478C>T
ENST00000646891.1:c.1902C>T	ENSP00000493543.1:p.Ser634=
ENST00000647434.1:c.779C>T	ENSP00000495132.1:p.Ala260Val
ENST00000288602.10:c.1902C>T	ENSP00000288602.6:p.Ser634=
ENST00000479537.5:c.186C>T	ENSP00000418033.1:p.Ser62=
ENST00000496384.6:c.725C>T
ENST00000497784.1:c.1937C>T	ENSP00000420119.1:n.1937C>T
NM_004333.4:c.1902C>T , LRG_299t1:c.1902C>T	NP_004324.2:p.Ser634=
XM_005250045.1:c.1902C>T	XP_005250102.1:p.Ser634=
XM_005250046.1:c.1902C>T	XP_005250103.1:p.Ser634=
XM_011516529.1:c.1902C>T	XP_011514831.1:p.Ser634=
XM_011516530.1:c.1736C>T	XP_011514832.1:p.Ala579Val
XR_242190.1:n.1910C>T
XR_927520.1:n.1910C>T
XR_927521.1:n.1910C>T
XR_927522.1:n.1744C>T
XR_927523.1:n.1744C>T
NM_001354609.1:c.1902C>T	NP_001341538.1:p.Ser634=
NM_004333.5:c.1902C>T	NP_004324.2:p.Ser634=
NR_148928.1:n.3000C>T
XM_017012558.1:c.2022C>T	XP_016868047.1:p.Ser674=
XM_017012559.1:c.2022C>T	XP_016868048.1:p.Ser674=
XR_001744857.1:n.2030C>T
XR_001744858.1:n.1864C>T
NM_001354609.2:c.1902C>T	NP_001341538.1:p.Ser634=
NM_001374244.1:c.2022C>T	NP_001361173.1:p.Ser674=
NM_001374258.1:c.2022C>T MANE Plus Clinical	NP_001361187.1:p.Ser674=
NM_004333.6:c.1902C>T MANE Select	NP_004324.2:p.Ser634=
NM_001378467.1:c.1911C>T	NP_001365396.1:p.Ser637=
NM_001378468.1:c.1902C>T	NP_001365397.1:p.Ser634=
NM_001378469.1:c.1836C>T	NP_001365398.1:p.Ser612=
NM_001378470.1:c.1800C>T	NP_001365399.1:p.Ser600=
NM_001378471.1:c.1791C>T	NP_001365400.1:p.Ser597=
NM_001378472.1:c.1746C>T	NP_001365401.1:p.Ser582=
NM_001378473.1:c.1746C>T	NP_001365402.1:p.Ser582=
NM_001378474.1:c.1902C>T	NP_001365403.1:p.Ser634=
NM_001378475.1:c.1638C>T	NP_001365404.1:p.Ser546=