Canonical Allele Identifier: CA168048164
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs909262796

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754108T>G , CM000669.2:g.140754108T>G GRCh38
NC_000007.13:g.140453908T>G , CM000669.1:g.140453908T>G GRCh37
NC_000007.12:g.140100377T>G NCBI36
NG_007873.3:g.175657A>C , LRG_299:g.175657A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1741+79A>C MANE Select ENSP00000493543.1:n.1741+79A>C
ENST00000288602.11:c.1861+79A>C ENSP00000288602.7:n.1861+79A>C
ENST00000479537.6:c.411+79A>C
ENST00000496384.7:c.1741+79A>C ENSP00000419060.2:n.1741+79A>C
ENST00000497784.2:c.*1191+79A>C ENSP00000420119.2:n.*1191+79A>C
ENST00000642228.1:c.*819+79A>C ENSP00000493678.1:n.*819+79A>C
ENST00000642875.1:n.1259-4690A>C
ENST00000644120.1:n.2131+79A>C
ENST00000644650.1:c.837+79A>C
ENST00000644905.1:n.1909A>C
ENST00000644969.2:c.1861+79A>C MANE Plus Clinical ENSP00000496776.1:n.1861+79A>C
ENST00000646730.1:c.*317+79A>C ENSP00000494784.1:n.*317+79A>C
ENST00000646891.1:c.1741+79A>C ENSP00000493543.1:n.1741+79A>C
ENST00000647434.1:c.738-4690A>C ENSP00000495132.1:n.738-4690A>C
ENST00000288602.10:c.1741+79A>C ENSP00000288602.6:n.1741+79A>C
ENST00000479537.5:c.25+79A>C ENSP00000418033.1:n.25+79A>C
ENST00000496384.6:c.564+79A>C
ENST00000497784.1:c.1776+79A>C ENSP00000420119.1:n.1776+79A>C
NM_004333.4:c.1741+79A>C , LRG_299t1:c.1741+79A>C NP_004324.2:n.1741+79A>C
XM_005250045.1:c.1741+79A>C XP_005250102.1:n.1741+79A>C
XM_005250046.1:c.1741+79A>C XP_005250103.1:n.1741+79A>C
XM_011516529.1:c.1741+79A>C XP_011514831.1:n.1741+79A>C
XM_011516530.1:c.1695-4690A>C XP_011514832.1:n.1695-4690A>C
XR_242190.1:n.1749+79A>C
XR_927520.1:n.1749+79A>C
XR_927521.1:n.1749+79A>C
XR_927522.1:n.1703-4690A>C
XR_927523.1:n.1703-4690A>C
NM_001354609.1:c.1741+79A>C NP_001341538.1:n.1741+79A>C
NM_004333.5:c.1741+79A>C NP_004324.2:n.1741+79A>C
NR_148928.1:n.2125A>C
XM_017012558.1:c.1861+79A>C XP_016868047.1:n.1861+79A>C
XM_017012559.1:c.1861+79A>C XP_016868048.1:n.1861+79A>C
XR_001744857.1:n.1869+79A>C
XR_001744858.1:n.1823-4690A>C
NM_001354609.2:c.1741+79A>C NP_001341538.1:n.1741+79A>C
NM_001374244.1:c.1861+79A>C NP_001361173.1:n.1861+79A>C
NM_001374258.1:c.1861+79A>C MANE Plus Clinical NP_001361187.1:n.1861+79A>C
NM_004333.6:c.1741+79A>C MANE Select NP_004324.2:n.1741+79A>C
NM_001378467.1:c.1750+79A>C NP_001365396.1:n.1750+79A>C
NM_001378468.1:c.1741+79A>C NP_001365397.1:n.1741+79A>C
NM_001378469.1:c.1675+79A>C NP_001365398.1:n.1675+79A>C
NM_001378470.1:c.1639+79A>C NP_001365399.1:n.1639+79A>C
NM_001378471.1:c.1630+79A>C NP_001365400.1:n.1630+79A>C
NM_001378472.1:c.1585+79A>C NP_001365401.1:n.1585+79A>C
NM_001378473.1:c.1585+79A>C NP_001365402.1:n.1585+79A>C
NM_001378474.1:c.1741+79A>C NP_001365403.1:n.1741+79A>C
NM_001378475.1:c.1477+79A>C NP_001365404.1:n.1477+79A>C