Canonical Allele Identifier: CA891841835

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727423_54727476del , CM000666.2:g.54727423_54727476del	GRCh38
NC_000004.11:g.55593589_55593642del , CM000666.1:g.55593589_55593642del	GRCh37
NC_000004.10:g.55288346_55288399del	NCBI36
NG_007456.1:g.74429_74482del , LRG_307:g.74429_74482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1646_1699del	ENSP00000390987.3:p.Met549_Tyr567delinsAsn
ENST00000685269.1:n.1733_1786del
ENST00000686011.1:c.1643_1696del	ENSP00000509704.1:p.Met548_Tyr566delinsAsn
ENST00000687109.1:c.1658_1711del	ENSP00000509371.1:p.Met553_Tyr571delinsAsn
ENST00000687208.1:n.2070_2123del
ENST00000687246.1:c.1643_1696del	ENSP00000509114.1:p.Met548_Tyr566delinsAsn
ENST00000687265.1:n.1813_1866del
ENST00000687295.1:c.1643_1696del	ENSP00000509450.1:p.Met548_Tyr566delinsAsn
ENST00000689832.1:c.1658_1711del	ENSP00000509084.1:p.Met553_Tyr571delinsAsn
ENST00000689994.1:c.1145_1198del	ENSP00000509156.1:p.Met382_Tyr400delinsAsn
ENST00000690543.1:c.1646_1699del	ENSP00000508831.1:p.Met549_Tyr567delinsAsn
ENST00000690917.1:n.1873_1926del
ENST00000691361.1:n.565_618del
ENST00000692783.1:c.1655_1708del	ENSP00000508733.1:p.Met552_Tyr570delinsAsn
ENST00000692991.1:n.1752_1805del
ENST00000288135.6:c.1655_1708del MANE Select	ENSP00000288135.6:p.Met552_Tyr570delinsAsn
ENST00000288135.5:c.1655_1708del	ENSP00000288135.5:p.Met552_Tyr570delinsAsn
ENST00000412167.6:c.1643_1696del	ENSP00000390987.2:p.Met548_Tyr566delinsAsn
NM_000222.2:c.1655_1708del , LRG_307t1:c.1655_1708del	NP_000213.1:p.Met552_Tyr570delinsAsn
NM_001093772.1:c.1643_1696del	NP_001087241.1:p.Met548_Tyr566delinsAsn
XM_005265740.1:c.1658_1711del	XP_005265797.1:p.Met553_Tyr571delinsAsn
XM_005265741.1:c.1658_1711del	XP_005265798.1:p.Met553_Tyr571delinsAsn
XM_005265742.1:c.1646_1699del	XP_005265799.1:p.Met549_Tyr567delinsAsn
XM_005265742.3:c.1646_1699del	XP_005265799.1:p.Met549_Tyr567delinsAsn
XM_017008178.1:c.1655_1708del	XP_016863667.1:p.Met552_Tyr570delinsAsn
XM_017008179.1:c.1646_1699del	XP_016863668.1:p.Met549_Tyr567delinsAsn
XM_017008180.1:c.1643_1696del	XP_016863669.1:p.Met548_Tyr566delinsAsn
NM_000222.3:c.1655_1708del MANE Select	NP_000213.1:p.Met552_Tyr570delinsAsn
NM_001093772.2:c.1643_1696del	NP_001087241.1:p.Met548_Tyr566delinsAsn
NM_001385284.1:c.1658_1711del	NP_001372213.1:p.Met553_Tyr571delinsAsn
NM_001385285.1:c.1655_1708del	NP_001372214.1:p.Met552_Tyr570delinsAsn
NM_001385286.1:c.1643_1696del	NP_001372215.1:p.Met548_Tyr566delinsAsn
NM_001385288.1:c.1646_1699del	NP_001372217.1:p.Met549_Tyr567delinsAsn
NM_001385290.1:c.1658_1711del	NP_001372219.1:p.Met553_Tyr571delinsAsn
NM_001385292.1:c.1646_1699del	NP_001372221.1:p.Met549_Tyr567delinsAsn