Canonical Allele Identifier: CA1747725921

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776811_140776812delinsTA , CM000669.2:g.140776811_140776812delinsTA	GRCh38
NC_000007.13:g.140476611_140476612delinsTA , CM000669.1:g.140476611_140476612delinsTA	GRCh37
NC_000007.12:g.140123080_140123081delinsTA	NCBI36
NG_007873.3:g.152953_152954delinsTA , LRG_299:g.152953_152954delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1694+100_1694+101delinsTA MANE Select	ENSP00000493543.1:n.1694+100_1694+101delinsTA
ENST00000288602.11:c.1814+100_1814+101delinsTA	ENSP00000288602.7:n.1814+100_1814+101delinsTA
ENST00000479537.6:c.364+100_364+101delinsTA
ENST00000496384.7:c.1694+100_1694+101delinsTA	ENSP00000419060.2:n.1694+100_1694+101delinsTA
ENST00000497784.2:c.*1144+100_*1144+101delinsTA	ENSP00000420119.2:n.*1144+100_*1144+101delinsTA
ENST00000642228.1:c.*772+100_*772+101delinsTA	ENSP00000493678.1:n.*772+100_*772+101delinsTA
ENST00000642875.1:n.1258+100_1258+101delinsTA
ENST00000644120.1:n.2084+100_2084+101delinsTA
ENST00000644650.1:c.790+100_790+101delinsTA
ENST00000644905.1:n.1783+100_1783+101delinsTA
ENST00000644969.2:c.1814+100_1814+101delinsTA MANE Plus Clinical	ENSP00000496776.1:n.1814+100_1814+101delinsTA
ENST00000646730.1:c.1694+100_1694+101delinsTA	ENSP00000494784.1:n.1694+100_1694+101delinsTA
ENST00000646891.1:c.1694+100_1694+101delinsTA	ENSP00000493543.1:n.1694+100_1694+101delinsTA
ENST00000647434.1:c.737+100_737+101delinsTA	ENSP00000495132.1:n.737+100_737+101delinsTA
ENST00000288602.10:c.1694+100_1694+101delinsTA	ENSP00000288602.6:n.1694+100_1694+101delinsTA
ENST00000496384.6:c.517+100_517+101delinsTA
ENST00000497784.1:c.1729+100_1729+101delinsTA	ENSP00000420119.1:n.1729+100_1729+101delinsTA
NM_004333.4:c.1694+100_1694+101delinsTA , LRG_299t1:c.1694+100_1694+101delinsTA	NP_004324.2:n.1694+100_1694+101delinsTA
XM_005250045.1:c.1694+100_1694+101delinsTA	XP_005250102.1:n.1694+100_1694+101delinsTA
XM_005250046.1:c.1694+100_1694+101delinsTA	XP_005250103.1:n.1694+100_1694+101delinsTA
XM_011516529.1:c.1694+100_1694+101delinsTA	XP_011514831.1:n.1694+100_1694+101delinsTA
XM_011516530.1:c.1694+100_1694+101delinsTA	XP_011514832.1:n.1694+100_1694+101delinsTA
XR_242190.1:n.1702+100_1702+101delinsTA
XR_927520.1:n.1702+100_1702+101delinsTA
XR_927521.1:n.1702+100_1702+101delinsTA
XR_927522.1:n.1702+100_1702+101delinsTA
XR_927523.1:n.1702+100_1702+101delinsTA
NM_001354609.1:c.1694+100_1694+101delinsTA	NP_001341538.1:n.1694+100_1694+101delinsTA
NM_004333.5:c.1694+100_1694+101delinsTA	NP_004324.2:n.1694+100_1694+101delinsTA
NR_148928.1:n.1999+100_1999+101delinsTA
XM_017012558.1:c.1814+100_1814+101delinsTA	XP_016868047.1:n.1814+100_1814+101delinsTA
XM_017012559.1:c.1814+100_1814+101delinsTA	XP_016868048.1:n.1814+100_1814+101delinsTA
XR_001744857.1:n.1822+100_1822+101delinsTA
XR_001744858.1:n.1822+100_1822+101delinsTA
NM_001354609.2:c.1694+100_1694+101delinsTA	NP_001341538.1:n.1694+100_1694+101delinsTA
NM_001374244.1:c.1814+100_1814+101delinsTA	NP_001361173.1:n.1814+100_1814+101delinsTA
NM_001374258.1:c.1814+100_1814+101delinsTA MANE Plus Clinical	NP_001361187.1:n.1814+100_1814+101delinsTA
NM_004333.6:c.1694+100_1694+101delinsTA MANE Select	NP_004324.2:n.1694+100_1694+101delinsTA
NM_001378467.1:c.1703+100_1703+101delinsTA	NP_001365396.1:n.1703+100_1703+101delinsTA
NM_001378468.1:c.1694+100_1694+101delinsTA	NP_001365397.1:n.1694+100_1694+101delinsTA
NM_001378469.1:c.1628+100_1628+101delinsTA	NP_001365398.1:n.1628+100_1628+101delinsTA
NM_001378470.1:c.1592+100_1592+101delinsTA	NP_001365399.1:n.1592+100_1592+101delinsTA
NM_001378471.1:c.1583+100_1583+101delinsTA	NP_001365400.1:n.1583+100_1583+101delinsTA
NM_001378472.1:c.1538+100_1538+101delinsTA	NP_001365401.1:n.1538+100_1538+101delinsTA
NM_001378473.1:c.1538+100_1538+101delinsTA	NP_001365402.1:n.1538+100_1538+101delinsTA
NM_001378474.1:c.1694+100_1694+101delinsTA	NP_001365403.1:n.1694+100_1694+101delinsTA
NM_001378475.1:c.1430+100_1430+101delinsTA	NP_001365404.1:n.1430+100_1430+101delinsTA