Canonical Allele Identifier: CA2761715274

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736692_54736693del , CM000666.2:g.54736692_54736693del	GRCh38
NC_000004.11:g.55602858_55602859del , CM000666.1:g.55602858_55602859del	GRCh37
NC_000004.10:g.55297615_55297616del	NCBI36
NG_007456.1:g.83698_83699del , LRG_307:g.83698_83699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2585-29_2585-28del	ENSP00000390987.3:n.2585-29_2585-28del
ENST00000684818.1:n.1289-29_1289-28del
ENST00000685269.1:n.2675-29_2675-28del
ENST00000686011.1:c.2582-29_2582-28del	ENSP00000509704.1:n.2582-29_2582-28del
ENST00000687109.1:c.2600-29_2600-28del	ENSP00000509371.1:n.2600-29_2600-28del
ENST00000687208.1:n.3009-29_3009-28del
ENST00000687246.1:c.2462-29_2462-28del	ENSP00000509114.1:n.2462-29_2462-28del
ENST00000687265.1:n.2755-29_2755-28del
ENST00000687295.1:c.2585-29_2585-28del	ENSP00000509450.1:n.2585-29_2585-28del
ENST00000688060.1:n.394-29_394-28del
ENST00000689832.1:c.2597-29_2597-28del	ENSP00000509084.1:n.2597-29_2597-28del
ENST00000689994.1:c.2087-29_2087-28del	ENSP00000509156.1:n.2087-29_2087-28del
ENST00000690543.1:c.2588-29_2588-28del	ENSP00000508831.1:n.2588-29_2588-28del
ENST00000690917.1:n.2815-29_2815-28del
ENST00000691361.1:n.1507-29_1507-28del
ENST00000692301.1:n.1289-29_1289-28del
ENST00000692783.1:c.2594-29_2594-28del	ENSP00000508733.1:n.2594-29_2594-28del
ENST00000692991.1:n.2694-29_2694-28del
ENST00000288135.6:c.2597-29_2597-28del MANE Select	ENSP00000288135.6:n.2597-29_2597-28del
ENST00000288135.5:c.2597-29_2597-28del	ENSP00000288135.5:n.2597-29_2597-28del
ENST00000412167.6:c.2585-29_2585-28del	ENSP00000390987.2:n.2585-29_2585-28del
NM_000222.2:c.2597-29_2597-28del , LRG_307t1:c.2597-29_2597-28del	NP_000213.1:n.2597-29_2597-28del
NM_001093772.1:c.2585-29_2585-28del	NP_001087241.1:n.2585-29_2585-28del
XM_005265740.1:c.2600-29_2600-28del	XP_005265797.1:n.2600-29_2600-28del
XM_005265741.1:c.2597-29_2597-28del	XP_005265798.1:n.2597-29_2597-28del
XM_005265742.1:c.2588-29_2588-28del	XP_005265799.1:n.2588-29_2588-28del
XM_005265742.3:c.2588-29_2588-28del	XP_005265799.1:n.2588-29_2588-28del
XM_017008178.1:c.2594-29_2594-28del	XP_016863667.1:n.2594-29_2594-28del
XM_017008179.1:c.2585-29_2585-28del	XP_016863668.1:n.2585-29_2585-28del
XM_017008180.1:c.2582-29_2582-28del	XP_016863669.1:n.2582-29_2582-28del
NM_000222.3:c.2597-29_2597-28del MANE Select	NP_000213.1:n.2597-29_2597-28del
NM_001093772.2:c.2585-29_2585-28del	NP_001087241.1:n.2585-29_2585-28del
NM_001385284.1:c.2600-29_2600-28del	NP_001372213.1:n.2600-29_2600-28del
NM_001385285.1:c.2594-29_2594-28del	NP_001372214.1:n.2594-29_2594-28del
NM_001385286.1:c.2582-29_2582-28del	NP_001372215.1:n.2582-29_2582-28del
NM_001385288.1:c.2588-29_2588-28del	NP_001372217.1:n.2588-29_2588-28del
NM_001385290.1:c.2597-29_2597-28del	NP_001372219.1:n.2597-29_2597-28del
NM_001385292.1:c.2585-29_2585-28del	NP_001372221.1:n.2585-29_2585-28del