Canonical Allele Identifier: CA356907834

Gene: KIT

Linked Data

• ClinVar Variation Id: 2720695
• ClinVar RCV Id: RCV003526793
• dbSNP Id: rs375351432
• MyVariant Identifiers: chr4:g.55593995C>A (hg19) ; chr4:g.54727829C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727829C>A , CM000666.2:g.54727829C>A	GRCh38
NC_000004.11:g.55593995C>A , CM000666.1:g.55593995C>A	GRCh37
NC_000004.10:g.55288752C>A	NCBI36
NG_007456.1:g.74835C>A , LRG_307:g.74835C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1772C>A	ENSP00000390987.3:p.Thr591Asn
ENST00000685269.1:n.1859C>A
ENST00000686011.1:c.1769C>A	ENSP00000509704.1:p.Thr590Asn
ENST00000687109.1:c.1784C>A	ENSP00000509371.1:p.Thr595Asn
ENST00000687208.1:n.2196C>A
ENST00000687246.1:c.1769C>A	ENSP00000509114.1:p.Thr590Asn
ENST00000687265.1:n.1939C>A
ENST00000687295.1:c.1769C>A	ENSP00000509450.1:p.Thr590Asn
ENST00000689832.1:c.1784C>A	ENSP00000509084.1:p.Thr595Asn
ENST00000689994.1:c.1271C>A	ENSP00000509156.1:p.Thr424Asn
ENST00000690543.1:c.1772C>A	ENSP00000508831.1:p.Thr591Asn
ENST00000690917.1:n.1999C>A
ENST00000691361.1:n.691C>A
ENST00000692783.1:c.1781C>A	ENSP00000508733.1:p.Thr594Asn
ENST00000692991.1:n.1878C>A
ENST00000288135.6:c.1781C>A MANE Select	ENSP00000288135.6:p.Thr594Asn
ENST00000288135.5:c.1781C>A	ENSP00000288135.5:p.Thr594Asn
ENST00000412167.6:c.1769C>A	ENSP00000390987.2:p.Thr590Asn
NM_000222.2:c.1781C>A , LRG_307t1:c.1781C>A	NP_000213.1:p.Thr594Asn
NM_001093772.1:c.1769C>A	NP_001087241.1:p.Thr590Asn
XM_005265740.1:c.1784C>A	XP_005265797.1:p.Thr595Asn
XM_005265741.1:c.1784C>A	XP_005265798.1:p.Thr595Asn
XM_005265742.1:c.1772C>A	XP_005265799.1:p.Thr591Asn
XM_005265742.3:c.1772C>A	XP_005265799.1:p.Thr591Asn
XM_017008178.1:c.1781C>A	XP_016863667.1:p.Thr594Asn
XM_017008179.1:c.1772C>A	XP_016863668.1:p.Thr591Asn
XM_017008180.1:c.1769C>A	XP_016863669.1:p.Thr590Asn
NM_000222.3:c.1781C>A MANE Select	NP_000213.1:p.Thr594Asn
NM_001093772.2:c.1769C>A	NP_001087241.1:p.Thr590Asn
NM_001385284.1:c.1784C>A	NP_001372213.1:p.Thr595Asn
NM_001385285.1:c.1781C>A	NP_001372214.1:p.Thr594Asn
NM_001385286.1:c.1769C>A	NP_001372215.1:p.Thr590Asn
NM_001385288.1:c.1772C>A	NP_001372217.1:p.Thr591Asn
NM_001385290.1:c.1784C>A	NP_001372219.1:p.Thr595Asn
NM_001385292.1:c.1772C>A	NP_001372221.1:p.Thr591Asn