Canonical Allele Identifier: CA16611682

Gene: KIT

Linked Data

• ClinVar Variation Id: 409757
• ClinVar RCV Id: RCV000471071 ; RCV003168816
• dbSNP Id: rs1060502557
• MyVariant Identifiers: chr4:g.55599356A>G (hg19) ; chr4:g.54733190A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733190A>G , CM000666.2:g.54733190A>G	GRCh38
NC_000004.11:g.55599356A>G , CM000666.1:g.55599356A>G	GRCh37
NC_000004.10:g.55294113A>G	NCBI36
NG_007456.1:g.80196A>G , LRG_307:g.80196A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2470A>G	ENSP00000390987.3:p.Asn824Asp
ENST00000685269.1:n.2560A>G
ENST00000686011.1:c.2467A>G	ENSP00000509704.1:p.Asn823Asp
ENST00000687109.1:c.2485A>G	ENSP00000509371.1:p.Asn829Asp
ENST00000687208.1:n.2894A>G
ENST00000687246.1:c.2349+1192A>G	ENSP00000509114.1:n.2349+1192A>G
ENST00000687265.1:n.2640A>G
ENST00000687295.1:c.2470A>G	ENSP00000509450.1:p.Asn824Asp
ENST00000688060.1:n.279A>G
ENST00000688704.1:n.1494A>G
ENST00000689832.1:c.2482A>G	ENSP00000509084.1:p.Asn828Asp
ENST00000689994.1:c.1972A>G	ENSP00000509156.1:p.Asn658Asp
ENST00000690543.1:c.2473A>G	ENSP00000508831.1:p.Asn825Asp
ENST00000690917.1:n.2700A>G
ENST00000691361.1:n.1392A>G
ENST00000692783.1:c.2479A>G	ENSP00000508733.1:p.Asn827Asp
ENST00000692991.1:n.2579A>G
ENST00000288135.6:c.2482A>G MANE Select	ENSP00000288135.6:p.Asn828Asp
ENST00000288135.5:c.2482A>G	ENSP00000288135.5:p.Asn828Asp
ENST00000412167.6:c.2470A>G	ENSP00000390987.2:p.Asn824Asp
ENST00000512959.1:n.535A>G
NM_000222.2:c.2482A>G , LRG_307t1:c.2482A>G	NP_000213.1:p.Asn828Asp
NM_001093772.1:c.2470A>G	NP_001087241.1:p.Asn824Asp
XM_005265740.1:c.2485A>G	XP_005265797.1:p.Asn829Asp
XM_005265741.1:c.2482A>G	XP_005265798.1:p.Asn828Asp
XM_005265742.1:c.2473A>G	XP_005265799.1:p.Asn825Asp
XM_005265742.3:c.2473A>G	XP_005265799.1:p.Asn825Asp
XM_017008178.1:c.2479A>G	XP_016863667.1:p.Asn827Asp
XM_017008179.1:c.2470A>G	XP_016863668.1:p.Asn824Asp
XM_017008180.1:c.2467A>G	XP_016863669.1:p.Asn823Asp
NM_000222.3:c.2482A>G MANE Select	NP_000213.1:p.Asn828Asp
NM_001093772.2:c.2470A>G	NP_001087241.1:p.Asn824Asp
NM_001385284.1:c.2485A>G	NP_001372213.1:p.Asn829Asp
NM_001385285.1:c.2479A>G	NP_001372214.1:p.Asn827Asp
NM_001385286.1:c.2467A>G	NP_001372215.1:p.Asn823Asp
NM_001385288.1:c.2473A>G	NP_001372217.1:p.Asn825Asp
NM_001385290.1:c.2482A>G	NP_001372219.1:p.Asn828Asp
NM_001385292.1:c.2470A>G	NP_001372221.1:p.Asn824Asp