Canonical Allele Identifier: CA439291329

Gene: KIT

Linked Data

• ClinVar Variation Id: 1556007
• ClinVar RCV Id: RCV002185468
• dbSNP Id: rs2109779476
• MyVariant Identifiers: chr4:g.55594011T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727845T>C , CM000666.2:g.54727845T>C	GRCh38
NC_000004.11:g.55594011T>C , CM000666.1:g.55594011T>C	GRCh37
NC_000004.10:g.55288768T>C	NCBI36
NG_007456.1:g.74851T>C , LRG_307:g.74851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1788T>C	ENSP00000390987.3:p.Ala596=
ENST00000685269.1:n.1875T>C
ENST00000686011.1:c.1785T>C	ENSP00000509704.1:p.Ala595=
ENST00000687109.1:c.1800T>C	ENSP00000509371.1:p.Ala600=
ENST00000687208.1:n.2212T>C
ENST00000687246.1:c.1785T>C	ENSP00000509114.1:p.Ala595=
ENST00000687265.1:n.1955T>C
ENST00000687295.1:c.1785T>C	ENSP00000509450.1:p.Ala595=
ENST00000689832.1:c.1800T>C	ENSP00000509084.1:p.Ala600=
ENST00000689994.1:c.1287T>C	ENSP00000509156.1:p.Ala429=
ENST00000690543.1:c.1788T>C	ENSP00000508831.1:p.Ala596=
ENST00000690917.1:n.2015T>C
ENST00000691361.1:n.707T>C
ENST00000692783.1:c.1797T>C	ENSP00000508733.1:p.Ala599=
ENST00000692991.1:n.1894T>C
ENST00000288135.6:c.1797T>C MANE Select	ENSP00000288135.6:p.Ala599=
ENST00000288135.5:c.1797T>C	ENSP00000288135.5:p.Ala599=
ENST00000412167.6:c.1785T>C	ENSP00000390987.2:p.Ala595=
NM_000222.2:c.1797T>C , LRG_307t1:c.1797T>C	NP_000213.1:p.Ala599=
NM_001093772.1:c.1785T>C	NP_001087241.1:p.Ala595=
XM_005265740.1:c.1800T>C	XP_005265797.1:p.Ala600=
XM_005265741.1:c.1800T>C	XP_005265798.1:p.Ala600=
XM_005265742.1:c.1788T>C	XP_005265799.1:p.Ala596=
XM_005265742.3:c.1788T>C	XP_005265799.1:p.Ala596=
XM_017008178.1:c.1797T>C	XP_016863667.1:p.Ala599=
XM_017008179.1:c.1788T>C	XP_016863668.1:p.Ala596=
XM_017008180.1:c.1785T>C	XP_016863669.1:p.Ala595=
NM_000222.3:c.1797T>C MANE Select	NP_000213.1:p.Ala599=
NM_001093772.2:c.1785T>C	NP_001087241.1:p.Ala595=
NM_001385284.1:c.1800T>C	NP_001372213.1:p.Ala600=
NM_001385285.1:c.1797T>C	NP_001372214.1:p.Ala599=
NM_001385286.1:c.1785T>C	NP_001372215.1:p.Ala595=
NM_001385288.1:c.1788T>C	NP_001372217.1:p.Ala596=
NM_001385290.1:c.1800T>C	NP_001372219.1:p.Ala600=
NM_001385292.1:c.1788T>C	NP_001372221.1:p.Ala596=