Canonical Allele Identifier: CA2685244390

Gene: BRAF

Linked Data

• gnomAD v4: 7-140801412-T-TCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801413_140801415dup , CM000669.2:g.140801413_140801415dup	GRCh38
NC_000007.13:g.140501213_140501215dup , CM000669.1:g.140501213_140501215dup	GRCh37
NC_000007.12:g.140147682_140147684dup	NCBI36
NG_007873.3:g.128350_128352dup , LRG_299:g.128350_128352dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.857_859dup MANE Select	ENSP00000493543.1:p.Leu286_Asp287insVal
ENST00000288602.11:c.857_859dup	ENSP00000288602.7:p.Leu286_Asp287insVal
ENST00000496384.7:c.857_859dup	ENSP00000419060.2:p.Leu286_Asp287insVal
ENST00000497784.2:c.*307_*309dup	ENSP00000420119.2:n.*307_*309dup
ENST00000642228.1:c.857_859dup	ENSP00000493678.1:p.Leu286_Asp287insVal
ENST00000642272.1:n.889_891dup
ENST00000642875.1:n.351_353dup
ENST00000643356.1:n.458_460dup
ENST00000644120.1:n.1299_1301dup
ENST00000644905.1:n.946_948dup
ENST00000644969.2:c.857_859dup MANE Plus Clinical	ENSP00000496776.1:p.Leu286_Asp287insVal
ENST00000646730.1:c.857_859dup	ENSP00000494784.1:p.Leu286_Asp287insVal
ENST00000646891.1:c.857_859dup	ENSP00000493543.1:p.Leu286_Asp287insVal
ENST00000288602.10:c.857_859dup	ENSP00000288602.6:p.Leu286_Asp287insVal
ENST00000497784.1:c.892_894dup	ENSP00000420119.1:n.892_894dup
NM_004333.4:c.857_859dup , LRG_299t1:c.857_859dup	NP_004324.2:p.Leu286_Asp287insVal
XM_005250045.1:c.857_859dup	XP_005250102.1:p.Leu286_Asp287insVal
XM_005250046.1:c.857_859dup	XP_005250103.1:p.Leu286_Asp287insVal
XM_011516529.1:c.857_859dup	XP_011514831.1:p.Leu286_Asp287insVal
XM_011516530.1:c.857_859dup	XP_011514832.1:p.Leu286_Asp287insVal
XR_242190.1:n.865_867dup
XR_927520.1:n.865_867dup
XR_927521.1:n.865_867dup
XR_927522.1:n.865_867dup
XR_927523.1:n.865_867dup
NM_001354609.1:c.857_859dup	NP_001341538.1:p.Leu286_Asp287insVal
NM_004333.5:c.857_859dup	NP_004324.2:p.Leu286_Asp287insVal
NR_148928.1:n.1162_1164dup
XM_017012558.1:c.857_859dup	XP_016868047.1:p.Leu286_Asp287insVal
XM_017012559.1:c.857_859dup	XP_016868048.1:p.Leu286_Asp287insVal
XR_001744857.1:n.865_867dup
XR_001744858.1:n.865_867dup
NM_001354609.2:c.857_859dup	NP_001341538.1:p.Leu286_Asp287insVal
NM_001374244.1:c.857_859dup	NP_001361173.1:p.Leu286_Asp287insVal
NM_001374258.1:c.857_859dup MANE Plus Clinical	NP_001361187.1:p.Leu286_Asp287insVal
NM_004333.6:c.857_859dup MANE Select	NP_004324.2:p.Leu286_Asp287insVal
NM_001378467.1:c.866_868dup	NP_001365396.1:p.Leu289_Asp290insVal
NM_001378468.1:c.857_859dup	NP_001365397.1:p.Leu286_Asp287insVal
NM_001378469.1:c.857_859dup	NP_001365398.1:p.Leu286_Asp287insVal
NM_001378470.1:c.755_757dup	NP_001365399.1:p.Leu252_Asp253insVal
NM_001378471.1:c.857_859dup	NP_001365400.1:p.Leu286_Asp287insVal
NM_001378472.1:c.701_703dup	NP_001365401.1:p.Leu234_Asp235insVal
NM_001378473.1:c.701_703dup	NP_001365402.1:p.Leu234_Asp235insVal
NM_001378474.1:c.857_859dup	NP_001365403.1:p.Leu286_Asp287insVal
NM_001378475.1:c.593_595dup	NP_001365404.1:p.Leu198_Asp199insVal