Canonical Allele Identifier: CA356907520

Gene: KIT

Linked Data

• ClinVar Variation Id: 579532
• ClinVar RCV Id: RCV000702843
• dbSNP Id: rs1016976398
• MyVariant Identifiers: chr4:g.55593634A>T (hg19) ; chr4:g.54727468A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727468A>T , CM000666.2:g.54727468A>T	GRCh38
NC_000004.11:g.55593634A>T , CM000666.1:g.55593634A>T	GRCh37
NC_000004.10:g.55288391A>T	NCBI36
NG_007456.1:g.74474A>T , LRG_307:g.74474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1691A>T	ENSP00000390987.3:p.Asn564Ile
ENST00000685269.1:n.1778A>T
ENST00000686011.1:c.1688A>T	ENSP00000509704.1:p.Asn563Ile
ENST00000687109.1:c.1703A>T	ENSP00000509371.1:p.Asn568Ile
ENST00000687208.1:n.2115A>T
ENST00000687246.1:c.1688A>T	ENSP00000509114.1:p.Asn563Ile
ENST00000687265.1:n.1858A>T
ENST00000687295.1:c.1688A>T	ENSP00000509450.1:p.Asn563Ile
ENST00000689832.1:c.1703A>T	ENSP00000509084.1:p.Asn568Ile
ENST00000689994.1:c.1190A>T	ENSP00000509156.1:p.Asn397Ile
ENST00000690543.1:c.1691A>T	ENSP00000508831.1:p.Asn564Ile
ENST00000690917.1:n.1918A>T
ENST00000691361.1:n.610A>T
ENST00000692783.1:c.1700A>T	ENSP00000508733.1:p.Asn567Ile
ENST00000692991.1:n.1797A>T
ENST00000288135.6:c.1700A>T MANE Select	ENSP00000288135.6:p.Asn567Ile
ENST00000288135.5:c.1700A>T	ENSP00000288135.5:p.Asn567Ile
ENST00000412167.6:c.1688A>T	ENSP00000390987.2:p.Asn563Ile
NM_000222.2:c.1700A>T , LRG_307t1:c.1700A>T	NP_000213.1:p.Asn567Ile
NM_001093772.1:c.1688A>T	NP_001087241.1:p.Asn563Ile
XM_005265740.1:c.1703A>T	XP_005265797.1:p.Asn568Ile
XM_005265741.1:c.1703A>T	XP_005265798.1:p.Asn568Ile
XM_005265742.1:c.1691A>T	XP_005265799.1:p.Asn564Ile
XM_005265742.3:c.1691A>T	XP_005265799.1:p.Asn564Ile
XM_017008178.1:c.1700A>T	XP_016863667.1:p.Asn567Ile
XM_017008179.1:c.1691A>T	XP_016863668.1:p.Asn564Ile
XM_017008180.1:c.1688A>T	XP_016863669.1:p.Asn563Ile
NM_000222.3:c.1700A>T MANE Select	NP_000213.1:p.Asn567Ile
NM_001093772.2:c.1688A>T	NP_001087241.1:p.Asn563Ile
NM_001385284.1:c.1703A>T	NP_001372213.1:p.Asn568Ile
NM_001385285.1:c.1700A>T	NP_001372214.1:p.Asn567Ile
NM_001385286.1:c.1688A>T	NP_001372215.1:p.Asn563Ile
NM_001385288.1:c.1691A>T	NP_001372217.1:p.Asn564Ile
NM_001385290.1:c.1703A>T	NP_001372219.1:p.Asn568Ile
NM_001385292.1:c.1691A>T	NP_001372221.1:p.Asn564Ile