Canonical Allele Identifier: CA369538559

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439736A>G (hg19) ; chr7:g.140739936A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739936A>G , CM000669.2:g.140739936A>G	GRCh38
NC_000007.13:g.140439736A>G , CM000669.1:g.140439736A>G	GRCh37
NC_000007.12:g.140086205A>G	NCBI36
NG_007873.3:g.189829T>C , LRG_299:g.189829T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2003T>C MANE Select	ENSP00000493543.1:p.Met668Thr
ENST00000288602.11:c.2123T>C	ENSP00000288602.7:p.Met708Thr
ENST00000479537.6:c.755T>C
ENST00000496384.7:c.2003T>C	ENSP00000419060.2:p.Met668Thr
ENST00000497784.2:c.*1453T>C	ENSP00000420119.2:n.*1453T>C
ENST00000642228.1:c.*1081T>C	ENSP00000493678.1:n.*1081T>C
ENST00000642875.1:n.1401T>C
ENST00000644120.1:n.2393T>C
ENST00000644650.1:c.1302T>C
ENST00000644905.1:n.2885T>C
ENST00000644969.2:c.2123T>C MANE Plus Clinical	ENSP00000496776.1:p.Met708Thr
ENST00000645443.1:n.1782T>C
ENST00000646730.1:c.*661T>C	ENSP00000494784.1:n.*661T>C
ENST00000646891.1:c.2003T>C	ENSP00000493543.1:p.Met668Thr
ENST00000647434.1:c.880T>C	ENSP00000495132.1:n.880T>C
ENST00000288602.10:c.2003T>C	ENSP00000288602.6:p.Met668Thr
ENST00000479537.5:c.369T>C	ENSP00000418033.1:n.369T>C
ENST00000496384.6:c.826T>C
ENST00000497784.1:c.2038T>C	ENSP00000420119.1:n.2038T>C
NM_004333.4:c.2003T>C , LRG_299t1:c.2003T>C	NP_004324.2:p.Met668Thr
XM_005250045.1:c.2003T>C	XP_005250102.1:p.Met668Thr
XM_005250046.1:c.2003T>C	XP_005250103.1:p.Met668Thr
XM_011516529.1:c.2003T>C	XP_011514831.1:p.Met668Thr
XR_242190.1:n.2093T>C
XR_927520.1:n.2132T>C
XR_927521.1:n.2214T>C
XR_927522.1:n.1845T>C
XR_927523.1:n.1927T>C
NM_001354609.1:c.2003T>C	NP_001341538.1:p.Met668Thr
NM_004333.5:c.2003T>C	NP_004324.2:p.Met668Thr
NR_148928.1:n.3101T>C
XM_017012558.1:c.2123T>C	XP_016868047.1:p.Met708Thr
XM_017012559.1:c.2123T>C	XP_016868048.1:p.Met708Thr
XR_001744857.1:n.2213T>C
XR_001744858.1:n.1965T>C
NM_001354609.2:c.2003T>C	NP_001341538.1:p.Met668Thr
NM_001374244.1:c.2123T>C	NP_001361173.1:p.Met708Thr
NM_001374258.1:c.2123T>C MANE Plus Clinical	NP_001361187.1:p.Met708Thr
NM_004333.6:c.2003T>C MANE Select	NP_004324.2:p.Met668Thr
NM_001378467.1:c.2012T>C	NP_001365396.1:p.Met671Thr
NM_001378468.1:c.2003T>C	NP_001365397.1:p.Met668Thr
NM_001378469.1:c.1937T>C	NP_001365398.1:p.Met646Thr
NM_001378470.1:c.1901T>C	NP_001365399.1:p.Met634Thr
NM_001378471.1:c.1892T>C	NP_001365400.1:p.Met631Thr
NM_001378472.1:c.1847T>C	NP_001365401.1:p.Met616Thr
NM_001378473.1:c.1847T>C	NP_001365402.1:p.Met616Thr
NM_001378474.1:c.2003T>C	NP_001365403.1:p.Met668Thr
NM_001378475.1:c.1739T>C	NP_001365404.1:p.Met580Thr