Canonical Allele Identifier: CA2685240938

Gene: BRAF

Linked Data

• gnomAD v4: 7-140776835-ATAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776836_140776838del , CM000669.2:g.140776836_140776838del	GRCh38
NC_000007.13:g.140476636_140476638del , CM000669.1:g.140476636_140476638del	GRCh37
NC_000007.12:g.140123105_140123107del	NCBI36
NG_007873.3:g.152927_152929del , LRG_299:g.152927_152929del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1694+74_1694+76del MANE Select	ENSP00000493543.1:n.1694+74_1694+76del
ENST00000288602.11:c.1814+74_1814+76del	ENSP00000288602.7:n.1814+74_1814+76del
ENST00000479537.6:c.364+74_364+76del
ENST00000496384.7:c.1694+74_1694+76del	ENSP00000419060.2:n.1694+74_1694+76del
ENST00000497784.2:c.*1144+74_*1144+76del	ENSP00000420119.2:n.*1144+74_*1144+76del
ENST00000642228.1:c.*772+74_*772+76del	ENSP00000493678.1:n.*772+74_*772+76del
ENST00000642875.1:n.1258+74_1258+76del
ENST00000644120.1:n.2084+74_2084+76del
ENST00000644650.1:c.790+74_790+76del
ENST00000644905.1:n.1783+74_1783+76del
ENST00000644969.2:c.1814+74_1814+76del MANE Plus Clinical	ENSP00000496776.1:n.1814+74_1814+76del
ENST00000646730.1:c.1694+74_1694+76del	ENSP00000494784.1:n.1694+74_1694+76del
ENST00000646891.1:c.1694+74_1694+76del	ENSP00000493543.1:n.1694+74_1694+76del
ENST00000647434.1:c.737+74_737+76del	ENSP00000495132.1:n.737+74_737+76del
ENST00000288602.10:c.1694+74_1694+76del	ENSP00000288602.6:n.1694+74_1694+76del
ENST00000496384.6:c.517+74_517+76del
ENST00000497784.1:c.1729+74_1729+76del	ENSP00000420119.1:n.1729+74_1729+76del
NM_004333.4:c.1694+74_1694+76del , LRG_299t1:c.1694+74_1694+76del	NP_004324.2:n.1694+74_1694+76del
XM_005250045.1:c.1694+74_1694+76del	XP_005250102.1:n.1694+74_1694+76del
XM_005250046.1:c.1694+74_1694+76del	XP_005250103.1:n.1694+74_1694+76del
XM_011516529.1:c.1694+74_1694+76del	XP_011514831.1:n.1694+74_1694+76del
XM_011516530.1:c.1694+74_1694+76del	XP_011514832.1:n.1694+74_1694+76del
XR_242190.1:n.1702+74_1702+76del
XR_927520.1:n.1702+74_1702+76del
XR_927521.1:n.1702+74_1702+76del
XR_927522.1:n.1702+74_1702+76del
XR_927523.1:n.1702+74_1702+76del
NM_001354609.1:c.1694+74_1694+76del	NP_001341538.1:n.1694+74_1694+76del
NM_004333.5:c.1694+74_1694+76del	NP_004324.2:n.1694+74_1694+76del
NR_148928.1:n.1999+74_1999+76del
XM_017012558.1:c.1814+74_1814+76del	XP_016868047.1:n.1814+74_1814+76del
XM_017012559.1:c.1814+74_1814+76del	XP_016868048.1:n.1814+74_1814+76del
XR_001744857.1:n.1822+74_1822+76del
XR_001744858.1:n.1822+74_1822+76del
NM_001354609.2:c.1694+74_1694+76del	NP_001341538.1:n.1694+74_1694+76del
NM_001374244.1:c.1814+74_1814+76del	NP_001361173.1:n.1814+74_1814+76del
NM_001374258.1:c.1814+74_1814+76del MANE Plus Clinical	NP_001361187.1:n.1814+74_1814+76del
NM_004333.6:c.1694+74_1694+76del MANE Select	NP_004324.2:n.1694+74_1694+76del
NM_001378467.1:c.1703+74_1703+76del	NP_001365396.1:n.1703+74_1703+76del
NM_001378468.1:c.1694+74_1694+76del	NP_001365397.1:n.1694+74_1694+76del
NM_001378469.1:c.1628+74_1628+76del	NP_001365398.1:n.1628+74_1628+76del
NM_001378470.1:c.1592+74_1592+76del	NP_001365399.1:n.1592+74_1592+76del
NM_001378471.1:c.1583+74_1583+76del	NP_001365400.1:n.1583+74_1583+76del
NM_001378472.1:c.1538+74_1538+76del	NP_001365401.1:n.1538+74_1538+76del
NM_001378473.1:c.1538+74_1538+76del	NP_001365402.1:n.1538+74_1538+76del
NM_001378474.1:c.1694+74_1694+76del	NP_001365403.1:n.1694+74_1694+76del
NM_001378475.1:c.1430+74_1430+76del	NP_001365404.1:n.1430+74_1430+76del