Canonical Allele Identifier: CA356906436

Gene: KIT

Linked Data

• ClinVar Variation Id: 1060447
• ClinVar RCV Id: RCV001369882
• dbSNP Id: rs1331885453
• MyVariant Identifiers: chr4:g.55592131C>A (hg19) ; chr4:g.54725965C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54725965C>A , CM000666.2:g.54725965C>A	GRCh38
NC_000004.11:g.55592131C>A , CM000666.1:g.55592131C>A	GRCh37
NC_000004.10:g.55286888C>A	NCBI36
NG_007456.1:g.72971C>A , LRG_307:g.72971C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1458C>A	ENSP00000390987.3:p.His486Gln
ENST00000685269.1:n.1533C>A
ENST00000685816.1:c.393C>A	ENSP00000508749.1:p.His131Gln
ENST00000686011.1:c.1455C>A	ENSP00000509704.1:p.His485Gln
ENST00000687109.1:c.1458C>A	ENSP00000509371.1:p.His486Gln
ENST00000687208.1:n.1870C>A
ENST00000687246.1:c.1455C>A	ENSP00000509114.1:p.His485Gln
ENST00000687265.1:n.1625C>A
ENST00000687295.1:c.1455C>A	ENSP00000509450.1:p.His485Gln
ENST00000689832.1:c.1458C>A	ENSP00000509084.1:p.His486Gln
ENST00000689994.1:c.945C>A	ENSP00000509156.1:p.His315Gln
ENST00000690543.1:c.1458C>A	ENSP00000508831.1:p.His486Gln
ENST00000690917.1:n.1673C>A
ENST00000691361.1:n.377C>A
ENST00000692783.1:c.1455C>A	ENSP00000508733.1:p.His485Gln
ENST00000692991.1:n.1564C>A
ENST00000288135.6:c.1455C>A MANE Select	ENSP00000288135.6:p.His485Gln
ENST00000288135.5:c.1455C>A	ENSP00000288135.5:p.His485Gln
ENST00000412167.6:c.1455C>A	ENSP00000390987.2:p.His485Gln
NM_000222.2:c.1455C>A , LRG_307t1:c.1455C>A	NP_000213.1:p.His485Gln
NM_001093772.1:c.1455C>A	NP_001087241.1:p.His485Gln
XM_005265740.1:c.1458C>A	XP_005265797.1:p.His486Gln
XM_005265741.1:c.1458C>A	XP_005265798.1:p.His486Gln
XM_005265742.1:c.1458C>A	XP_005265799.1:p.His486Gln
XM_005265742.3:c.1458C>A	XP_005265799.1:p.His486Gln
XM_017008178.1:c.1455C>A	XP_016863667.1:p.His485Gln
XM_017008179.1:c.1458C>A	XP_016863668.1:p.His486Gln
XM_017008180.1:c.1455C>A	XP_016863669.1:p.His485Gln
NM_000222.3:c.1455C>A MANE Select	NP_000213.1:p.His485Gln
NM_001093772.2:c.1455C>A	NP_001087241.1:p.His485Gln
NM_001385284.1:c.1458C>A	NP_001372213.1:p.His486Gln
NM_001385285.1:c.1455C>A	NP_001372214.1:p.His485Gln
NM_001385286.1:c.1455C>A	NP_001372215.1:p.His485Gln
NM_001385288.1:c.1458C>A	NP_001372217.1:p.His486Gln
NM_001385290.1:c.1458C>A	NP_001372219.1:p.His486Gln
NM_001385292.1:c.1458C>A	NP_001372221.1:p.His486Gln