Canonical Allele Identifier: CA145581

Gene: BRAF

Linked Data

• ClinVar Variation Id: 41445
• ClinVar RCV Id: RCV000034331 ; RCV000077864 ; RCV000370547 ; RCV000406169 ; RCV001811235
• dbSNP Id: rs71645935
• ExAC: 7:140624522 G / A
• gnomAD v2: 7-140624522-G-A
• gnomAD v3: 7-140924722-G-A
• gnomAD v4: 7-140924722-G-A
• MyVariant Identifiers: chr7:g.140624522G>A (hg19) ; chr7:g.140924722G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140924722G>A , CM000669.2:g.140924722G>A	GRCh38
NC_000007.13:g.140624522G>A , CM000669.1:g.140624522G>A	GRCh37
NC_000007.12:g.140270991G>A	NCBI36
NG_007873.3:g.5043C>T , LRG_299:g.5043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.-19C>T MANE Select	ENSP00000493543.1:n.-19C>T
ENST00000288602.11:c.-19C>T	ENSP00000288602.7:n.-19C>T
ENST00000469930.2:c.-19C>T	ENSP00000495858.1:n.-19C>T
ENST00000496384.7:c.-19C>T	ENSP00000419060.2:n.-19C>T
ENST00000642272.1:n.5C>T
ENST00000644969.2:c.-19C>T MANE Plus Clinical	ENSP00000496776.1:n.-19C>T
ENST00000646891.1:c.-19C>T	ENSP00000493543.1:n.-19C>T
ENST00000288602.10:c.-19C>T	ENSP00000288602.6:n.-19C>T
NM_004333.4:c.-19C>T , LRG_299t1:c.-19C>T	NP_004324.2:n.-19C>T
NM_001354609.1:c.-19C>T	NP_001341538.1:n.-19C>T
NM_004333.5:c.-19C>T	NP_004324.2:n.-19C>T
NR_148928.1:n.207C>T
NM_001354609.2:c.-19C>T	NP_001341538.1:n.-19C>T
NM_001374244.1:c.-19C>T	NP_001361173.1:n.-19C>T
NM_001374258.1:c.-19C>T MANE Plus Clinical	NP_001361187.1:n.-19C>T
NM_004333.6:c.-19C>T MANE Select	NP_004324.2:n.-19C>T
NM_001378467.1:c.-19C>T	NP_001365396.1:n.-19C>T
NM_001378468.1:c.-19C>T	NP_001365397.1:n.-19C>T
NM_001378469.1:c.-19C>T	NP_001365398.1:n.-19C>T
NM_001378470.1:c.-19C>T	NP_001365399.1:n.-19C>T
NM_001378471.1:c.-19C>T	NP_001365400.1:n.-19C>T
NM_001378474.1:c.-19C>T	NP_001365403.1:n.-19C>T
NM_001378475.1:c.-19C>T	NP_001365404.1:n.-19C>T