Canonical Allele Identifier: CA2761715271

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736687_54736689del , CM000666.2:g.54736687_54736689del	GRCh38
NC_000004.11:g.55602853_55602855del , CM000666.1:g.55602853_55602855del	GRCh37
NC_000004.10:g.55297610_55297612del	NCBI36
NG_007456.1:g.83693_83695del , LRG_307:g.83693_83695del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2585-34_2585-32del	ENSP00000390987.3:n.2585-34_2585-32del
ENST00000684818.1:n.1289-34_1289-32del
ENST00000685269.1:n.2675-34_2675-32del
ENST00000686011.1:c.2582-34_2582-32del	ENSP00000509704.1:n.2582-34_2582-32del
ENST00000687109.1:c.2600-34_2600-32del	ENSP00000509371.1:n.2600-34_2600-32del
ENST00000687208.1:n.3009-34_3009-32del
ENST00000687246.1:c.2462-34_2462-32del	ENSP00000509114.1:n.2462-34_2462-32del
ENST00000687265.1:n.2755-34_2755-32del
ENST00000687295.1:c.2585-34_2585-32del	ENSP00000509450.1:n.2585-34_2585-32del
ENST00000688060.1:n.394-34_394-32del
ENST00000689832.1:c.2597-34_2597-32del	ENSP00000509084.1:n.2597-34_2597-32del
ENST00000689994.1:c.2087-34_2087-32del	ENSP00000509156.1:n.2087-34_2087-32del
ENST00000690543.1:c.2588-34_2588-32del	ENSP00000508831.1:n.2588-34_2588-32del
ENST00000690917.1:n.2815-34_2815-32del
ENST00000691361.1:n.1507-34_1507-32del
ENST00000692301.1:n.1289-34_1289-32del
ENST00000692783.1:c.2594-34_2594-32del	ENSP00000508733.1:n.2594-34_2594-32del
ENST00000692991.1:n.2694-34_2694-32del
ENST00000288135.6:c.2597-34_2597-32del MANE Select	ENSP00000288135.6:n.2597-34_2597-32del
ENST00000288135.5:c.2597-34_2597-32del	ENSP00000288135.5:n.2597-34_2597-32del
ENST00000412167.6:c.2585-34_2585-32del	ENSP00000390987.2:n.2585-34_2585-32del
NM_000222.2:c.2597-34_2597-32del , LRG_307t1:c.2597-34_2597-32del	NP_000213.1:n.2597-34_2597-32del
NM_001093772.1:c.2585-34_2585-32del	NP_001087241.1:n.2585-34_2585-32del
XM_005265740.1:c.2600-34_2600-32del	XP_005265797.1:n.2600-34_2600-32del
XM_005265741.1:c.2597-34_2597-32del	XP_005265798.1:n.2597-34_2597-32del
XM_005265742.1:c.2588-34_2588-32del	XP_005265799.1:n.2588-34_2588-32del
XM_005265742.3:c.2588-34_2588-32del	XP_005265799.1:n.2588-34_2588-32del
XM_017008178.1:c.2594-34_2594-32del	XP_016863667.1:n.2594-34_2594-32del
XM_017008179.1:c.2585-34_2585-32del	XP_016863668.1:n.2585-34_2585-32del
XM_017008180.1:c.2582-34_2582-32del	XP_016863669.1:n.2582-34_2582-32del
NM_000222.3:c.2597-34_2597-32del MANE Select	NP_000213.1:n.2597-34_2597-32del
NM_001093772.2:c.2585-34_2585-32del	NP_001087241.1:n.2585-34_2585-32del
NM_001385284.1:c.2600-34_2600-32del	NP_001372213.1:n.2600-34_2600-32del
NM_001385285.1:c.2594-34_2594-32del	NP_001372214.1:n.2594-34_2594-32del
NM_001385286.1:c.2582-34_2582-32del	NP_001372215.1:n.2582-34_2582-32del
NM_001385288.1:c.2588-34_2588-32del	NP_001372217.1:n.2588-34_2588-32del
NM_001385290.1:c.2597-34_2597-32del	NP_001372219.1:n.2597-34_2597-32del
NM_001385292.1:c.2585-34_2585-32del	NP_001372221.1:n.2585-34_2585-32del