Canonical Allele Identifier: CA356907805

Gene: KIT

Linked Data

• ClinVar Variation Id: 1480836
• ClinVar RCV Id: RCV001994035
• dbSNP Id: rs2109779212
• MyVariant Identifiers: chr4:g.55593989G>T (hg19) ; chr4:g.54727823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727823G>T , CM000666.2:g.54727823G>T	GRCh38
NC_000004.11:g.55593989G>T , CM000666.1:g.55593989G>T	GRCh37
NC_000004.10:g.55288746G>T	NCBI36
NG_007456.1:g.74829G>T , LRG_307:g.74829G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1766G>T	ENSP00000390987.3:p.Gly589Val
ENST00000685269.1:n.1853G>T
ENST00000686011.1:c.1763G>T	ENSP00000509704.1:p.Gly588Val
ENST00000687109.1:c.1778G>T	ENSP00000509371.1:p.Gly593Val
ENST00000687208.1:n.2190G>T
ENST00000687246.1:c.1763G>T	ENSP00000509114.1:p.Gly588Val
ENST00000687265.1:n.1933G>T
ENST00000687295.1:c.1763G>T	ENSP00000509450.1:p.Gly588Val
ENST00000689832.1:c.1778G>T	ENSP00000509084.1:p.Gly593Val
ENST00000689994.1:c.1265G>T	ENSP00000509156.1:p.Gly422Val
ENST00000690543.1:c.1766G>T	ENSP00000508831.1:p.Gly589Val
ENST00000690917.1:n.1993G>T
ENST00000691361.1:n.685G>T
ENST00000692783.1:c.1775G>T	ENSP00000508733.1:p.Gly592Val
ENST00000692991.1:n.1872G>T
ENST00000288135.6:c.1775G>T MANE Select	ENSP00000288135.6:p.Gly592Val
ENST00000288135.5:c.1775G>T	ENSP00000288135.5:p.Gly592Val
ENST00000412167.6:c.1763G>T	ENSP00000390987.2:p.Gly588Val
NM_000222.2:c.1775G>T , LRG_307t1:c.1775G>T	NP_000213.1:p.Gly592Val
NM_001093772.1:c.1763G>T	NP_001087241.1:p.Gly588Val
XM_005265740.1:c.1778G>T	XP_005265797.1:p.Gly593Val
XM_005265741.1:c.1778G>T	XP_005265798.1:p.Gly593Val
XM_005265742.1:c.1766G>T	XP_005265799.1:p.Gly589Val
XM_005265742.3:c.1766G>T	XP_005265799.1:p.Gly589Val
XM_017008178.1:c.1775G>T	XP_016863667.1:p.Gly592Val
XM_017008179.1:c.1766G>T	XP_016863668.1:p.Gly589Val
XM_017008180.1:c.1763G>T	XP_016863669.1:p.Gly588Val
NM_000222.3:c.1775G>T MANE Select	NP_000213.1:p.Gly592Val
NM_001093772.2:c.1763G>T	NP_001087241.1:p.Gly588Val
NM_001385284.1:c.1778G>T	NP_001372213.1:p.Gly593Val
NM_001385285.1:c.1775G>T	NP_001372214.1:p.Gly592Val
NM_001385286.1:c.1763G>T	NP_001372215.1:p.Gly588Val
NM_001385288.1:c.1766G>T	NP_001372217.1:p.Gly589Val
NM_001385290.1:c.1778G>T	NP_001372219.1:p.Gly593Val
NM_001385292.1:c.1766G>T	NP_001372221.1:p.Gly589Val