Canonical Allele Identifier: CA1747732090

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800463_140800464delinsCT , CM000669.2:g.140800463_140800464delinsCT	GRCh38
NC_000007.13:g.140500263_140500264delinsCT , CM000669.1:g.140500263_140500264delinsCT	GRCh37
NC_000007.12:g.140146732_140146733delinsCT	NCBI36
NG_007873.3:g.129301_129302delinsAG , LRG_299:g.129301_129302delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.878_879delinsAG MANE Select	ENSP00000493543.1:p.Lys293=
ENST00000288602.11:c.878_879delinsAG	ENSP00000288602.7:p.Lys293=
ENST00000496384.7:c.878_879delinsAG	ENSP00000419060.2:p.Lys293=
ENST00000497784.2:c.*328_*329delinsAG	ENSP00000420119.2:n.*328_*329delinsAG
ENST00000642228.1:c.861-2_861-1delinsAG	ENSP00000493678.1:n.861-2_861-1delinsAG
ENST00000642272.1:n.910_911delinsAG
ENST00000642875.1:n.372_373delinsAG
ENST00000644120.1:n.1320_1321delinsAG
ENST00000644905.1:n.967_968delinsAG
ENST00000644969.2:c.878_879delinsAG MANE Plus Clinical	ENSP00000496776.1:p.Lys293=
ENST00000646730.1:c.878_879delinsAG	ENSP00000494784.1:p.Lys293=
ENST00000646891.1:c.878_879delinsAG	ENSP00000493543.1:p.Lys293=
ENST00000288602.10:c.878_879delinsAG	ENSP00000288602.6:p.Lys293=
ENST00000497784.1:c.913_914delinsAG	ENSP00000420119.1:n.913_914delinsAG
NM_004333.4:c.878_879delinsAG , LRG_299t1:c.878_879delinsAG	NP_004324.2:p.Lys293=
XM_005250045.1:c.878_879delinsAG	XP_005250102.1:p.Lys293=
XM_005250046.1:c.878_879delinsAG	XP_005250103.1:p.Lys293=
XM_011516529.1:c.878_879delinsAG	XP_011514831.1:p.Lys293=
XM_011516530.1:c.878_879delinsAG	XP_011514832.1:p.Lys293=
XR_242190.1:n.886_887delinsAG
XR_927520.1:n.886_887delinsAG
XR_927521.1:n.886_887delinsAG
XR_927522.1:n.886_887delinsAG
XR_927523.1:n.886_887delinsAG
NM_001354609.1:c.878_879delinsAG	NP_001341538.1:p.Lys293=
NM_004333.5:c.878_879delinsAG	NP_004324.2:p.Lys293=
NR_148928.1:n.1183_1184delinsAG
XM_017012558.1:c.878_879delinsAG	XP_016868047.1:p.Lys293=
XM_017012559.1:c.878_879delinsAG	XP_016868048.1:p.Lys293=
XR_001744857.1:n.886_887delinsAG
XR_001744858.1:n.886_887delinsAG
NM_001354609.2:c.878_879delinsAG	NP_001341538.1:p.Lys293=
NM_001374244.1:c.878_879delinsAG	NP_001361173.1:p.Lys293=
NM_001374258.1:c.878_879delinsAG MANE Plus Clinical	NP_001361187.1:p.Lys293=
NM_004333.6:c.878_879delinsAG MANE Select	NP_004324.2:p.Lys293=
NM_001378467.1:c.887_888delinsAG	NP_001365396.1:p.Lys296=
NM_001378468.1:c.878_879delinsAG	NP_001365397.1:p.Lys293=
NM_001378469.1:c.878_879delinsAG	NP_001365398.1:p.Lys293=
NM_001378470.1:c.776_777delinsAG	NP_001365399.1:p.Lys259=
NM_001378471.1:c.878_879delinsAG	NP_001365400.1:p.Lys293=
NM_001378472.1:c.722_723delinsAG	NP_001365401.1:p.Lys241=
NM_001378473.1:c.722_723delinsAG	NP_001365402.1:p.Lys241=
NM_001378474.1:c.878_879delinsAG	NP_001365403.1:p.Lys293=
NM_001378475.1:c.614_615delinsAG	NP_001365404.1:p.Lys205=