Canonical Allele Identifier: CA1458747304

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736683_54736684delinsTC , CM000666.2:g.54736683_54736684delinsTC	GRCh38
NC_000004.11:g.55602849_55602850delinsTC , CM000666.1:g.55602849_55602850delinsTC	GRCh37
NC_000004.10:g.55297606_55297607delinsTC	NCBI36
NG_007456.1:g.83689_83690delinsTC , LRG_307:g.83689_83690delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2585-38_2585-37delinsTC	ENSP00000390987.3:n.2585-38_2585-37delinsTC
ENST00000684818.1:n.1289-38_1289-37delinsTC
ENST00000685269.1:n.2675-38_2675-37delinsTC
ENST00000686011.1:c.2582-38_2582-37delinsTC	ENSP00000509704.1:n.2582-38_2582-37delinsTC
ENST00000687109.1:c.2600-38_2600-37delinsTC	ENSP00000509371.1:n.2600-38_2600-37delinsTC
ENST00000687208.1:n.3009-38_3009-37delinsTC
ENST00000687246.1:c.2462-38_2462-37delinsTC	ENSP00000509114.1:n.2462-38_2462-37delinsTC
ENST00000687265.1:n.2755-38_2755-37delinsTC
ENST00000687295.1:c.2585-38_2585-37delinsTC	ENSP00000509450.1:n.2585-38_2585-37delinsTC
ENST00000688060.1:n.394-38_394-37delinsTC
ENST00000689832.1:c.2597-38_2597-37delinsTC	ENSP00000509084.1:n.2597-38_2597-37delinsTC
ENST00000689994.1:c.2087-38_2087-37delinsTC	ENSP00000509156.1:n.2087-38_2087-37delinsTC
ENST00000690543.1:c.2588-38_2588-37delinsTC	ENSP00000508831.1:n.2588-38_2588-37delinsTC
ENST00000690917.1:n.2815-38_2815-37delinsTC
ENST00000691361.1:n.1507-38_1507-37delinsTC
ENST00000692301.1:n.1289-38_1289-37delinsTC
ENST00000692783.1:c.2594-38_2594-37delinsTC	ENSP00000508733.1:n.2594-38_2594-37delinsTC
ENST00000692991.1:n.2694-38_2694-37delinsTC
ENST00000288135.6:c.2597-38_2597-37delinsTC MANE Select	ENSP00000288135.6:n.2597-38_2597-37delinsTC
ENST00000288135.5:c.2597-38_2597-37delinsTC	ENSP00000288135.5:n.2597-38_2597-37delinsTC
ENST00000412167.6:c.2585-38_2585-37delinsTC	ENSP00000390987.2:n.2585-38_2585-37delinsTC
NM_000222.2:c.2597-38_2597-37delinsTC , LRG_307t1:c.2597-38_2597-37delinsTC	NP_000213.1:n.2597-38_2597-37delinsTC
NM_001093772.1:c.2585-38_2585-37delinsTC	NP_001087241.1:n.2585-38_2585-37delinsTC
XM_005265740.1:c.2600-38_2600-37delinsTC	XP_005265797.1:n.2600-38_2600-37delinsTC
XM_005265741.1:c.2597-38_2597-37delinsTC	XP_005265798.1:n.2597-38_2597-37delinsTC
XM_005265742.1:c.2588-38_2588-37delinsTC	XP_005265799.1:n.2588-38_2588-37delinsTC
XM_005265742.3:c.2588-38_2588-37delinsTC	XP_005265799.1:n.2588-38_2588-37delinsTC
XM_017008178.1:c.2594-38_2594-37delinsTC	XP_016863667.1:n.2594-38_2594-37delinsTC
XM_017008179.1:c.2585-38_2585-37delinsTC	XP_016863668.1:n.2585-38_2585-37delinsTC
XM_017008180.1:c.2582-38_2582-37delinsTC	XP_016863669.1:n.2582-38_2582-37delinsTC
NM_000222.3:c.2597-38_2597-37delinsTC MANE Select	NP_000213.1:n.2597-38_2597-37delinsTC
NM_001093772.2:c.2585-38_2585-37delinsTC	NP_001087241.1:n.2585-38_2585-37delinsTC
NM_001385284.1:c.2600-38_2600-37delinsTC	NP_001372213.1:n.2600-38_2600-37delinsTC
NM_001385285.1:c.2594-38_2594-37delinsTC	NP_001372214.1:n.2594-38_2594-37delinsTC
NM_001385286.1:c.2582-38_2582-37delinsTC	NP_001372215.1:n.2582-38_2582-37delinsTC
NM_001385288.1:c.2588-38_2588-37delinsTC	NP_001372217.1:n.2588-38_2588-37delinsTC
NM_001385290.1:c.2597-38_2597-37delinsTC	NP_001372219.1:n.2597-38_2597-37delinsTC
NM_001385292.1:c.2585-38_2585-37delinsTC	NP_001372221.1:n.2585-38_2585-37delinsTC