Canonical Allele Identifier: CA439291480
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1078602
ClinVar RCV Id: RCV001393589
dbSNP Id: rs1356154268
gnomAD v2: 4-55594226-C-T
gnomAD v4: 4-54728060-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54728060C>T , CM000666.2:g.54728060C>T GRCh38
NC_000004.11:g.55594226C>T , CM000666.1:g.55594226C>T GRCh37
NC_000004.10:g.55288983C>T NCBI36
NG_007456.1:g.75066C>T , LRG_307:g.75066C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1920C>T ENSP00000390987.3:p.Val640=
ENST00000685269.1:n.2007C>T
ENST00000686011.1:c.1917C>T ENSP00000509704.1:p.Val639=
ENST00000687109.1:c.1932C>T ENSP00000509371.1:p.Val644=
ENST00000687208.1:n.2344C>T
ENST00000687246.1:c.1917C>T ENSP00000509114.1:p.Val639=
ENST00000687265.1:n.2087C>T
ENST00000687295.1:c.1917C>T ENSP00000509450.1:p.Val639=
ENST00000689832.1:c.1932C>T ENSP00000509084.1:p.Val644=
ENST00000689994.1:c.1419C>T ENSP00000509156.1:p.Val473=
ENST00000690543.1:c.1920C>T ENSP00000508831.1:p.Val640=
ENST00000690917.1:n.2147C>T
ENST00000691361.1:n.839C>T
ENST00000692783.1:c.1929C>T ENSP00000508733.1:p.Val643=
ENST00000692991.1:n.2026C>T
ENST00000288135.6:c.1929C>T MANE Select ENSP00000288135.6:p.Val643=
ENST00000288135.5:c.1929C>T ENSP00000288135.5:p.Val643=
ENST00000412167.6:c.1917C>T ENSP00000390987.2:p.Val639=
NM_000222.2:c.1929C>T , LRG_307t1:c.1929C>T NP_000213.1:p.Val643=
NM_001093772.1:c.1917C>T NP_001087241.1:p.Val639=
XM_005265740.1:c.1932C>T XP_005265797.1:p.Val644=
XM_005265741.1:c.1932C>T XP_005265798.1:p.Val644=
XM_005265742.1:c.1920C>T XP_005265799.1:p.Val640=
XM_005265742.3:c.1920C>T XP_005265799.1:p.Val640=
XM_017008178.1:c.1929C>T XP_016863667.1:p.Val643=
XM_017008179.1:c.1920C>T XP_016863668.1:p.Val640=
XM_017008180.1:c.1917C>T XP_016863669.1:p.Val639=
NM_000222.3:c.1929C>T MANE Select NP_000213.1:p.Val643=
NM_001093772.2:c.1917C>T NP_001087241.1:p.Val639=
NM_001385284.1:c.1932C>T NP_001372213.1:p.Val644=
NM_001385285.1:c.1929C>T NP_001372214.1:p.Val643=
NM_001385286.1:c.1917C>T NP_001372215.1:p.Val639=
NM_001385288.1:c.1920C>T NP_001372217.1:p.Val640=
NM_001385290.1:c.1932C>T NP_001372219.1:p.Val644=
NM_001385292.1:c.1920C>T NP_001372221.1:p.Val640=