Canonical Allele Identifier: CA2923820

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736787G>A , CM000666.2:g.54736787G>A	GRCh38
NC_000004.11:g.55602953G>A , CM000666.1:g.55602953G>A	GRCh37
NC_000004.10:g.55297710G>A	NCBI36
NG_007456.1:g.83793G>A , LRG_307:g.83793G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000222.3:c.2663G>A MANE Select	NP_000213.1:p.Arg888Gln
ENST00000288135.6:c.2663G>A MANE Select	ENSP00000288135.6:p.Arg888Gln
NM_000222.2:c.2663G>A , LRG_307t1:c.2663G>A	NP_000213.1:p.Arg888Gln
NM_001093772.1:c.2651G>A	NP_001087241.1:p.Arg884Gln
NM_001093772.2:c.2651G>A	NP_001087241.1:p.Arg884Gln
NM_001385284.1:c.2666G>A	NP_001372213.1:p.Arg889Gln
NM_001385285.1:c.2660G>A	NP_001372214.1:p.Arg887Gln
NM_001385286.1:c.2648G>A	NP_001372215.1:p.Arg883Gln
NM_001385288.1:c.2654G>A	NP_001372217.1:p.Arg885Gln
NM_001385290.1:c.2663G>A	NP_001372219.1:p.Arg888Gln
NM_001385292.1:c.2651G>A	NP_001372221.1:p.Arg884Gln
ENST00000288135.5:c.2663G>A	ENSP00000288135.5:p.Arg888Gln
ENST00000412167.6:c.2651G>A	ENSP00000390987.2:p.Arg884Gln
ENST00000412167.7:c.2651G>A	ENSP00000390987.3:p.Arg884Gln
ENST00000684818.1:n.1355G>A
ENST00000685269.1:n.2741G>A
ENST00000686011.1:c.2648G>A	ENSP00000509704.1:p.Arg883Gln
ENST00000687109.1:c.2666G>A	ENSP00000509371.1:p.Arg889Gln
ENST00000687208.1:n.3075G>A
ENST00000687246.1:c.2528G>A	ENSP00000509114.1:p.Arg843Gln
ENST00000687265.1:n.2821G>A
ENST00000687295.1:c.2651G>A	ENSP00000509450.1:p.Arg884Gln
ENST00000688060.1:n.460G>A
ENST00000689832.1:c.2663G>A	ENSP00000509084.1:p.Arg888Gln
ENST00000689994.1:c.2153G>A	ENSP00000509156.1:p.Arg718Gln
ENST00000690543.1:c.2654G>A	ENSP00000508831.1:p.Arg885Gln
ENST00000690917.1:n.2881G>A
ENST00000691361.1:n.1573G>A
ENST00000692301.1:n.1355G>A
ENST00000692783.1:c.2660G>A	ENSP00000508733.1:p.Arg887Gln
ENST00000692991.1:n.2760G>A
XM_005265740.1:c.2666G>A	XP_005265797.1:p.Arg889Gln
XM_005265741.1:c.2663G>A	XP_005265798.1:p.Arg888Gln
XM_005265742.1:c.2654G>A	XP_005265799.1:p.Arg885Gln
XM_005265742.3:c.2654G>A	XP_005265799.1:p.Arg885Gln
XM_017008178.1:c.2660G>A	XP_016863667.1:p.Arg887Gln
XM_017008179.1:c.2651G>A	XP_016863668.1:p.Arg884Gln
XM_017008180.1:c.2648G>A	XP_016863669.1:p.Arg883Gln