Canonical Allele Identifier: CA439291316

Gene: KIT

Linked Data

• ClinVar Variation Id: 1155957
• ClinVar RCV Id: RCV001498470 ; RCV002405178
• dbSNP Id: rs2109779293
• MyVariant Identifiers: chr4:g.55593996C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727830C>T , CM000666.2:g.54727830C>T	GRCh38
NC_000004.11:g.55593996C>T , CM000666.1:g.55593996C>T	GRCh37
NC_000004.10:g.55288753C>T	NCBI36
NG_007456.1:g.74836C>T , LRG_307:g.74836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1773C>T	ENSP00000390987.3:p.Thr591=
ENST00000685269.1:n.1860C>T
ENST00000686011.1:c.1770C>T	ENSP00000509704.1:p.Thr590=
ENST00000687109.1:c.1785C>T	ENSP00000509371.1:p.Thr595=
ENST00000687208.1:n.2197C>T
ENST00000687246.1:c.1770C>T	ENSP00000509114.1:p.Thr590=
ENST00000687265.1:n.1940C>T
ENST00000687295.1:c.1770C>T	ENSP00000509450.1:p.Thr590=
ENST00000689832.1:c.1785C>T	ENSP00000509084.1:p.Thr595=
ENST00000689994.1:c.1272C>T	ENSP00000509156.1:p.Thr424=
ENST00000690543.1:c.1773C>T	ENSP00000508831.1:p.Thr591=
ENST00000690917.1:n.2000C>T
ENST00000691361.1:n.692C>T
ENST00000692783.1:c.1782C>T	ENSP00000508733.1:p.Thr594=
ENST00000692991.1:n.1879C>T
ENST00000288135.6:c.1782C>T MANE Select	ENSP00000288135.6:p.Thr594=
ENST00000288135.5:c.1782C>T	ENSP00000288135.5:p.Thr594=
ENST00000412167.6:c.1770C>T	ENSP00000390987.2:p.Thr590=
NM_000222.2:c.1782C>T , LRG_307t1:c.1782C>T	NP_000213.1:p.Thr594=
NM_001093772.1:c.1770C>T	NP_001087241.1:p.Thr590=
XM_005265740.1:c.1785C>T	XP_005265797.1:p.Thr595=
XM_005265741.1:c.1785C>T	XP_005265798.1:p.Thr595=
XM_005265742.1:c.1773C>T	XP_005265799.1:p.Thr591=
XM_005265742.3:c.1773C>T	XP_005265799.1:p.Thr591=
XM_017008178.1:c.1782C>T	XP_016863667.1:p.Thr594=
XM_017008179.1:c.1773C>T	XP_016863668.1:p.Thr591=
XM_017008180.1:c.1770C>T	XP_016863669.1:p.Thr590=
NM_000222.3:c.1782C>T MANE Select	NP_000213.1:p.Thr594=
NM_001093772.2:c.1770C>T	NP_001087241.1:p.Thr590=
NM_001385284.1:c.1785C>T	NP_001372213.1:p.Thr595=
NM_001385285.1:c.1782C>T	NP_001372214.1:p.Thr594=
NM_001385286.1:c.1770C>T	NP_001372215.1:p.Thr590=
NM_001385288.1:c.1773C>T	NP_001372217.1:p.Thr591=
NM_001385290.1:c.1785C>T	NP_001372219.1:p.Thr595=
NM_001385292.1:c.1773C>T	NP_001372221.1:p.Thr591=