Canonical Allele Identifier: CA834245694

Gene: BRAF

Linked Data

• dbSNP Id: rs1263302377
• gnomAD v4: 7-140753879-G-C
• MyVariant Identifiers: chr7:g.140453679G>C (hg19) ; chr7:g.140753879G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753879G>C , CM000669.2:g.140753879G>C	GRCh38
NC_000007.13:g.140453679G>C , CM000669.1:g.140453679G>C	GRCh37
NC_000007.12:g.140100148G>C	NCBI36
NG_007873.3:g.175886C>G , LRG_299:g.175886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1741+308C>G MANE Select	ENSP00000493543.1:n.1741+308C>G
ENST00000288602.11:c.1861+308C>G	ENSP00000288602.7:n.1861+308C>G
ENST00000479537.6:c.411+308C>G
ENST00000496384.7:c.1741+308C>G	ENSP00000419060.2:n.1741+308C>G
ENST00000497784.2:c.*1191+308C>G	ENSP00000420119.2:n.*1191+308C>G
ENST00000642228.1:c.*819+308C>G	ENSP00000493678.1:n.*819+308C>G
ENST00000642875.1:n.1259-4461C>G
ENST00000644120.1:n.2131+308C>G
ENST00000644650.1:c.837+308C>G
ENST00000644905.1:n.2138C>G
ENST00000644969.2:c.1861+308C>G MANE Plus Clinical	ENSP00000496776.1:n.1861+308C>G
ENST00000646730.1:c.*317+308C>G	ENSP00000494784.1:n.*317+308C>G
ENST00000646891.1:c.1741+308C>G	ENSP00000493543.1:n.1741+308C>G
ENST00000647434.1:c.738-4461C>G	ENSP00000495132.1:n.738-4461C>G
ENST00000288602.10:c.1741+308C>G	ENSP00000288602.6:n.1741+308C>G
ENST00000479537.5:c.25+308C>G	ENSP00000418033.1:n.25+308C>G
ENST00000496384.6:c.564+308C>G
ENST00000497784.1:c.1776+308C>G	ENSP00000420119.1:n.1776+308C>G
NM_004333.4:c.1741+308C>G , LRG_299t1:c.1741+308C>G	NP_004324.2:n.1741+308C>G
XM_005250045.1:c.1741+308C>G	XP_005250102.1:n.1741+308C>G
XM_005250046.1:c.1741+308C>G	XP_005250103.1:n.1741+308C>G
XM_011516529.1:c.1741+308C>G	XP_011514831.1:n.1741+308C>G
XM_011516530.1:c.1695-4461C>G	XP_011514832.1:n.1695-4461C>G
XR_242190.1:n.1749+308C>G
XR_927520.1:n.1749+308C>G
XR_927521.1:n.1749+308C>G
XR_927522.1:n.1703-4461C>G
XR_927523.1:n.1703-4461C>G
NM_001354609.1:c.1741+308C>G	NP_001341538.1:n.1741+308C>G
NM_004333.5:c.1741+308C>G	NP_004324.2:n.1741+308C>G
NR_148928.1:n.2354C>G
XM_017012558.1:c.1861+308C>G	XP_016868047.1:n.1861+308C>G
XM_017012559.1:c.1861+308C>G	XP_016868048.1:n.1861+308C>G
XR_001744857.1:n.1869+308C>G
XR_001744858.1:n.1823-4461C>G
NM_001354609.2:c.1741+308C>G	NP_001341538.1:n.1741+308C>G
NM_001374244.1:c.1861+308C>G	NP_001361173.1:n.1861+308C>G
NM_001374258.1:c.1861+308C>G MANE Plus Clinical	NP_001361187.1:n.1861+308C>G
NM_004333.6:c.1741+308C>G MANE Select	NP_004324.2:n.1741+308C>G
NM_001378467.1:c.1750+308C>G	NP_001365396.1:n.1750+308C>G
NM_001378468.1:c.1741+308C>G	NP_001365397.1:n.1741+308C>G
NM_001378469.1:c.1675+308C>G	NP_001365398.1:n.1675+308C>G
NM_001378470.1:c.1639+308C>G	NP_001365399.1:n.1639+308C>G
NM_001378471.1:c.1630+308C>G	NP_001365400.1:n.1630+308C>G
NM_001378472.1:c.1585+308C>G	NP_001365401.1:n.1585+308C>G
NM_001378473.1:c.1585+308C>G	NP_001365402.1:n.1585+308C>G
NM_001378474.1:c.1741+308C>G	NP_001365403.1:n.1741+308C>G
NM_001378475.1:c.1477+308C>G	NP_001365404.1:n.1477+308C>G