Canonical Allele Identifier: CA1458760439

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727057_54727059delinsCAA , CM000666.2:g.54727057_54727059delinsCAA	GRCh38
NC_000004.11:g.55593223_55593225delinsCAA , CM000666.1:g.55593223_55593225delinsCAA	GRCh37
NC_000004.10:g.55287980_55287982delinsCAA	NCBI36
NG_007456.1:g.74063_74065delinsCAA , LRG_307:g.74063_74065delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1532-161_1532-159delinsCAA	ENSP00000390987.3:n.1532-161_1532-159delinsCAA
ENST00000685269.1:n.1619-161_1619-159delinsCAA
ENST00000686011.1:c.1529-161_1529-159delinsCAA	ENSP00000509704.1:n.1529-161_1529-159delinsCAA
ENST00000687109.1:c.1544-161_1544-159delinsCAA	ENSP00000509371.1:n.1544-161_1544-159delinsCAA
ENST00000687208.1:n.1956-161_1956-159delinsCAA
ENST00000687246.1:c.1529-161_1529-159delinsCAA	ENSP00000509114.1:n.1529-161_1529-159delinsCAA
ENST00000687265.1:n.1699-161_1699-159delinsCAA
ENST00000687295.1:c.1529-161_1529-159delinsCAA	ENSP00000509450.1:n.1529-161_1529-159delinsCAA
ENST00000689832.1:c.1544-161_1544-159delinsCAA	ENSP00000509084.1:n.1544-161_1544-159delinsCAA
ENST00000689994.1:c.1031-161_1031-159delinsCAA	ENSP00000509156.1:n.1031-161_1031-159delinsCAA
ENST00000690543.1:c.1532-161_1532-159delinsCAA	ENSP00000508831.1:n.1532-161_1532-159delinsCAA
ENST00000690917.1:n.1759-161_1759-159delinsCAA
ENST00000691361.1:n.451-161_451-159delinsCAA
ENST00000692783.1:c.1541-161_1541-159delinsCAA	ENSP00000508733.1:n.1541-161_1541-159delinsCAA
ENST00000692991.1:n.1638-161_1638-159delinsCAA
ENST00000288135.6:c.1541-161_1541-159delinsCAA MANE Select	ENSP00000288135.6:n.1541-161_1541-159delinsCAA
ENST00000288135.5:c.1541-161_1541-159delinsCAA	ENSP00000288135.5:n.1541-161_1541-159delinsCAA
ENST00000412167.6:c.1529-161_1529-159delinsCAA	ENSP00000390987.2:n.1529-161_1529-159delinsCAA
NM_000222.2:c.1541-161_1541-159delinsCAA , LRG_307t1:c.1541-161_1541-159delinsCAA	NP_000213.1:n.1541-161_1541-159delinsCAA
NM_001093772.1:c.1529-161_1529-159delinsCAA	NP_001087241.1:n.1529-161_1529-159delinsCAA
XM_005265740.1:c.1544-161_1544-159delinsCAA	XP_005265797.1:n.1544-161_1544-159delinsCAA
XM_005265741.1:c.1544-161_1544-159delinsCAA	XP_005265798.1:n.1544-161_1544-159delinsCAA
XM_005265742.1:c.1532-161_1532-159delinsCAA	XP_005265799.1:n.1532-161_1532-159delinsCAA
XM_005265742.3:c.1532-161_1532-159delinsCAA	XP_005265799.1:n.1532-161_1532-159delinsCAA
XM_017008178.1:c.1541-161_1541-159delinsCAA	XP_016863667.1:n.1541-161_1541-159delinsCAA
XM_017008179.1:c.1532-161_1532-159delinsCAA	XP_016863668.1:n.1532-161_1532-159delinsCAA
XM_017008180.1:c.1529-161_1529-159delinsCAA	XP_016863669.1:n.1529-161_1529-159delinsCAA
NM_000222.3:c.1541-161_1541-159delinsCAA MANE Select	NP_000213.1:n.1541-161_1541-159delinsCAA
NM_001093772.2:c.1529-161_1529-159delinsCAA	NP_001087241.1:n.1529-161_1529-159delinsCAA
NM_001385284.1:c.1544-161_1544-159delinsCAA	NP_001372213.1:n.1544-161_1544-159delinsCAA
NM_001385285.1:c.1541-161_1541-159delinsCAA	NP_001372214.1:n.1541-161_1541-159delinsCAA
NM_001385286.1:c.1529-161_1529-159delinsCAA	NP_001372215.1:n.1529-161_1529-159delinsCAA
NM_001385288.1:c.1532-161_1532-159delinsCAA	NP_001372217.1:n.1532-161_1532-159delinsCAA
NM_001385290.1:c.1544-161_1544-159delinsCAA	NP_001372219.1:n.1544-161_1544-159delinsCAA
NM_001385292.1:c.1532-161_1532-159delinsCAA	NP_001372221.1:n.1532-161_1532-159delinsCAA