Canonical Allele Identifier: CA645516801

Gene: KIT

Linked Data

• COSMIC: COSM28994

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727435_54727483delinsCATC , CM000666.2:g.54727435_54727483delinsCATC	GRCh38
NC_000004.11:g.55593601_55593649delinsCATC , CM000666.1:g.55593601_55593649delinsCATC	GRCh37
NC_000004.10:g.55288358_55288406delinsCATC	NCBI36
NG_007456.1:g.74441_74489delinsCATC , LRG_307:g.74441_74489delinsCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1658_1706delinsCATC	ENSP00000390987.3:p.Gln553_Asp569delinsProSer
ENST00000685269.1:n.1745_1793delinsCATC
ENST00000686011.1:c.1655_1703delinsCATC	ENSP00000509704.1:p.Gln552_Asp568delinsProSer
ENST00000687109.1:c.1670_1718delinsCATC	ENSP00000509371.1:p.Gln557_Asp573delinsProSer
ENST00000687208.1:n.2082_2130delinsCATC
ENST00000687246.1:c.1655_1703delinsCATC	ENSP00000509114.1:p.Gln552_Asp568delinsProSer
ENST00000687265.1:n.1825_1873delinsCATC
ENST00000687295.1:c.1655_1703delinsCATC	ENSP00000509450.1:p.Gln552_Asp568delinsProSer
ENST00000689832.1:c.1670_1718delinsCATC	ENSP00000509084.1:p.Gln557_Asp573delinsProSer
ENST00000689994.1:c.1157_1205delinsCATC	ENSP00000509156.1:p.Gln386_Asp402delinsProSer
ENST00000690543.1:c.1658_1706delinsCATC	ENSP00000508831.1:p.Gln553_Asp569delinsProSer
ENST00000690917.1:n.1885_1933delinsCATC
ENST00000691361.1:n.577_625delinsCATC
ENST00000692783.1:c.1667_1715delinsCATC	ENSP00000508733.1:p.Gln556_Asp572delinsProSer
ENST00000692991.1:n.1764_1812delinsCATC
ENST00000288135.6:c.1667_1715delinsCATC MANE Select	ENSP00000288135.6:p.Gln556_Asp572delinsProSer
ENST00000288135.5:c.1667_1715delinsCATC	ENSP00000288135.5:p.Gln556_Asp572delinsProSer
ENST00000412167.6:c.1655_1703delinsCATC	ENSP00000390987.2:p.Gln552_Asp568delinsProSer
NM_000222.2:c.1667_1715delinsCATC , LRG_307t1:c.1667_1715delinsCATC	NP_000213.1:p.Gln556_Asp572delinsProSer
NM_001093772.1:c.1655_1703delinsCATC	NP_001087241.1:p.Gln552_Asp568delinsProSer
XM_005265740.1:c.1670_1718delinsCATC	XP_005265797.1:p.Gln557_Asp573delinsProSer
XM_005265741.1:c.1670_1718delinsCATC	XP_005265798.1:p.Gln557_Asp573delinsProSer
XM_005265742.1:c.1658_1706delinsCATC	XP_005265799.1:p.Gln553_Asp569delinsProSer
XM_005265742.3:c.1658_1706delinsCATC	XP_005265799.1:p.Gln553_Asp569delinsProSer
XM_017008178.1:c.1667_1715delinsCATC	XP_016863667.1:p.Gln556_Asp572delinsProSer
XM_017008179.1:c.1658_1706delinsCATC	XP_016863668.1:p.Gln553_Asp569delinsProSer
XM_017008180.1:c.1655_1703delinsCATC	XP_016863669.1:p.Gln552_Asp568delinsProSer
NM_000222.3:c.1667_1715delinsCATC MANE Select	NP_000213.1:p.Gln556_Asp572delinsProSer
NM_001093772.2:c.1655_1703delinsCATC	NP_001087241.1:p.Gln552_Asp568delinsProSer
NM_001385284.1:c.1670_1718delinsCATC	NP_001372213.1:p.Gln557_Asp573delinsProSer
NM_001385285.1:c.1667_1715delinsCATC	NP_001372214.1:p.Gln556_Asp572delinsProSer
NM_001385286.1:c.1655_1703delinsCATC	NP_001372215.1:p.Gln552_Asp568delinsProSer
NM_001385288.1:c.1658_1706delinsCATC	NP_001372217.1:p.Gln553_Asp569delinsProSer
NM_001385290.1:c.1670_1718delinsCATC	NP_001372219.1:p.Gln557_Asp573delinsProSer
NM_001385292.1:c.1658_1706delinsCATC	NP_001372221.1:p.Gln553_Asp569delinsProSer