Canonical Allele Identifier: CA1747710826

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140755194_140755195delinsTG , CM000669.2:g.140755194_140755195delinsTG	GRCh38
NC_000007.13:g.140454994_140454995delinsTG , CM000669.1:g.140454994_140454995delinsTG	GRCh37
NC_000007.12:g.140101463_140101464delinsTG	NCBI36
NG_007873.3:g.174570_174571delinsCA , LRG_299:g.174570_174571delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1695-962_1695-961delinsCA MANE Select	ENSP00000493543.1:n.1695-962_1695-961delinsCA
ENST00000288602.11:c.1815-962_1815-961delinsCA	ENSP00000288602.7:n.1815-962_1815-961delinsCA
ENST00000479537.6:c.365-962_365-961delinsCA
ENST00000496384.7:c.1695-962_1695-961delinsCA	ENSP00000419060.2:n.1695-962_1695-961delinsCA
ENST00000497784.2:c.*1145-962_*1145-961delinsCA	ENSP00000420119.2:n.*1145-962_*1145-961delinsCA
ENST00000642228.1:c.*773-962_*773-961delinsCA	ENSP00000493678.1:n.*773-962_*773-961delinsCA
ENST00000642875.1:n.1259-5777_1259-5776delinsCA
ENST00000644120.1:n.2085-962_2085-961delinsCA
ENST00000644650.1:c.791-962_791-961delinsCA
ENST00000644905.1:n.1784-962_1784-961delinsCA
ENST00000644969.2:c.1815-962_1815-961delinsCA MANE Plus Clinical	ENSP00000496776.1:n.1815-962_1815-961delinsCA
ENST00000646730.1:c.*271-962_*271-961delinsCA	ENSP00000494784.1:n.*271-962_*271-961delinsCA
ENST00000646891.1:c.1695-962_1695-961delinsCA	ENSP00000493543.1:n.1695-962_1695-961delinsCA
ENST00000647434.1:c.738-5777_738-5776delinsCA	ENSP00000495132.1:n.738-5777_738-5776delinsCA
ENST00000288602.10:c.1695-962_1695-961delinsCA	ENSP00000288602.6:n.1695-962_1695-961delinsCA
ENST00000496384.6:c.518-962_518-961delinsCA
ENST00000497784.1:c.1730-962_1730-961delinsCA	ENSP00000420119.1:n.1730-962_1730-961delinsCA
NM_004333.4:c.1695-962_1695-961delinsCA , LRG_299t1:c.1695-962_1695-961delinsCA	NP_004324.2:n.1695-962_1695-961delinsCA
XM_005250045.1:c.1695-962_1695-961delinsCA	XP_005250102.1:n.1695-962_1695-961delinsCA
XM_005250046.1:c.1695-962_1695-961delinsCA	XP_005250103.1:n.1695-962_1695-961delinsCA
XM_011516529.1:c.1695-962_1695-961delinsCA	XP_011514831.1:n.1695-962_1695-961delinsCA
XM_011516530.1:c.1695-5777_1695-5776delinsCA	XP_011514832.1:n.1695-5777_1695-5776delinsCA
XR_242190.1:n.1703-962_1703-961delinsCA
XR_927520.1:n.1703-962_1703-961delinsCA
XR_927521.1:n.1703-962_1703-961delinsCA
XR_927522.1:n.1703-5777_1703-5776delinsCA
XR_927523.1:n.1703-5777_1703-5776delinsCA
NM_001354609.1:c.1695-962_1695-961delinsCA	NP_001341538.1:n.1695-962_1695-961delinsCA
NM_004333.5:c.1695-962_1695-961delinsCA	NP_004324.2:n.1695-962_1695-961delinsCA
NR_148928.1:n.2000-962_2000-961delinsCA
XM_017012558.1:c.1815-962_1815-961delinsCA	XP_016868047.1:n.1815-962_1815-961delinsCA
XM_017012559.1:c.1815-962_1815-961delinsCA	XP_016868048.1:n.1815-962_1815-961delinsCA
XR_001744857.1:n.1823-962_1823-961delinsCA
XR_001744858.1:n.1823-5777_1823-5776delinsCA
NM_001354609.2:c.1695-962_1695-961delinsCA	NP_001341538.1:n.1695-962_1695-961delinsCA
NM_001374244.1:c.1815-962_1815-961delinsCA	NP_001361173.1:n.1815-962_1815-961delinsCA
NM_001374258.1:c.1815-962_1815-961delinsCA MANE Plus Clinical	NP_001361187.1:n.1815-962_1815-961delinsCA
NM_004333.6:c.1695-962_1695-961delinsCA MANE Select	NP_004324.2:n.1695-962_1695-961delinsCA
NM_001378467.1:c.1704-962_1704-961delinsCA	NP_001365396.1:n.1704-962_1704-961delinsCA
NM_001378468.1:c.1695-962_1695-961delinsCA	NP_001365397.1:n.1695-962_1695-961delinsCA
NM_001378469.1:c.1629-962_1629-961delinsCA	NP_001365398.1:n.1629-962_1629-961delinsCA
NM_001378470.1:c.1593-962_1593-961delinsCA	NP_001365399.1:n.1593-962_1593-961delinsCA
NM_001378471.1:c.1584-962_1584-961delinsCA	NP_001365400.1:n.1584-962_1584-961delinsCA
NM_001378472.1:c.1539-962_1539-961delinsCA	NP_001365401.1:n.1539-962_1539-961delinsCA
NM_001378473.1:c.1539-962_1539-961delinsCA	NP_001365402.1:n.1539-962_1539-961delinsCA
NM_001378474.1:c.1695-962_1695-961delinsCA	NP_001365403.1:n.1695-962_1695-961delinsCA
NM_001378475.1:c.1431-962_1431-961delinsCA	NP_001365404.1:n.1431-962_1431-961delinsCA