Canonical Allele Identifier: CA1458760549

Gene: KIT

Linked Data

• dbSNP Id: rs1722274116

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727154_54727157del , CM000666.2:g.54727154_54727157del	GRCh38
NC_000004.11:g.55593320_55593323del , CM000666.1:g.55593320_55593323del	GRCh37
NC_000004.10:g.55288077_55288080del	NCBI36
NG_007456.1:g.74160_74163del , LRG_307:g.74160_74163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1532-64_1532-61del	ENSP00000390987.3:n.1532-64_1532-61del
ENST00000685269.1:n.1619-64_1619-61del
ENST00000686011.1:c.1529-64_1529-61del	ENSP00000509704.1:n.1529-64_1529-61del
ENST00000687109.1:c.1544-64_1544-61del	ENSP00000509371.1:n.1544-64_1544-61del
ENST00000687208.1:n.1956-64_1956-61del
ENST00000687246.1:c.1529-64_1529-61del	ENSP00000509114.1:n.1529-64_1529-61del
ENST00000687265.1:n.1699-64_1699-61del
ENST00000687295.1:c.1529-64_1529-61del	ENSP00000509450.1:n.1529-64_1529-61del
ENST00000689832.1:c.1544-64_1544-61del	ENSP00000509084.1:n.1544-64_1544-61del
ENST00000689994.1:c.1031-64_1031-61del	ENSP00000509156.1:n.1031-64_1031-61del
ENST00000690543.1:c.1532-64_1532-61del	ENSP00000508831.1:n.1532-64_1532-61del
ENST00000690917.1:n.1759-64_1759-61del
ENST00000691361.1:n.451-64_451-61del
ENST00000692783.1:c.1541-64_1541-61del	ENSP00000508733.1:n.1541-64_1541-61del
ENST00000692991.1:n.1638-64_1638-61del
ENST00000288135.6:c.1541-64_1541-61del MANE Select	ENSP00000288135.6:n.1541-64_1541-61del
ENST00000288135.5:c.1541-64_1541-61del	ENSP00000288135.5:n.1541-64_1541-61del
ENST00000412167.6:c.1529-64_1529-61del	ENSP00000390987.2:n.1529-64_1529-61del
NM_000222.2:c.1541-64_1541-61del , LRG_307t1:c.1541-64_1541-61del	NP_000213.1:n.1541-64_1541-61del
NM_001093772.1:c.1529-64_1529-61del	NP_001087241.1:n.1529-64_1529-61del
XM_005265740.1:c.1544-64_1544-61del	XP_005265797.1:n.1544-64_1544-61del
XM_005265741.1:c.1544-64_1544-61del	XP_005265798.1:n.1544-64_1544-61del
XM_005265742.1:c.1532-64_1532-61del	XP_005265799.1:n.1532-64_1532-61del
XM_005265742.3:c.1532-64_1532-61del	XP_005265799.1:n.1532-64_1532-61del
XM_017008178.1:c.1541-64_1541-61del	XP_016863667.1:n.1541-64_1541-61del
XM_017008179.1:c.1532-64_1532-61del	XP_016863668.1:n.1532-64_1532-61del
XM_017008180.1:c.1529-64_1529-61del	XP_016863669.1:n.1529-64_1529-61del
NM_000222.3:c.1541-64_1541-61del MANE Select	NP_000213.1:n.1541-64_1541-61del
NM_001093772.2:c.1529-64_1529-61del	NP_001087241.1:n.1529-64_1529-61del
NM_001385284.1:c.1544-64_1544-61del	NP_001372213.1:n.1544-64_1544-61del
NM_001385285.1:c.1541-64_1541-61del	NP_001372214.1:n.1541-64_1541-61del
NM_001385286.1:c.1529-64_1529-61del	NP_001372215.1:n.1529-64_1529-61del
NM_001385288.1:c.1532-64_1532-61del	NP_001372217.1:n.1532-64_1532-61del
NM_001385290.1:c.1544-64_1544-61del	NP_001372219.1:n.1544-64_1544-61del
NM_001385292.1:c.1532-64_1532-61del	NP_001372221.1:n.1532-64_1532-61del