Canonical Allele Identifier: CA439291943
Gene: KIT HGNC NCBI

Linked Data

gnomAD v4: 4-54736503-A-G
MyVariant Identifiers: chr4:g.55602669A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736503A>G , CM000666.2:g.54736503A>G GRCh38
NC_000004.11:g.55602669A>G , CM000666.1:g.55602669A>G GRCh37
NC_000004.10:g.55297426A>G NCBI36
NG_007456.1:g.83509A>G , LRG_307:g.83509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2478A>G ENSP00000390987.3:p.Arg826=
ENST00000684818.1:n.1182A>G
ENST00000685269.1:n.2568A>G
ENST00000686011.1:c.2475A>G ENSP00000509704.1:p.Arg825=
ENST00000687109.1:c.2493A>G ENSP00000509371.1:p.Arg831=
ENST00000687208.1:n.2902A>G
ENST00000687246.1:c.2355A>G ENSP00000509114.1:p.Arg785=
ENST00000687265.1:n.2648A>G
ENST00000687295.1:c.2478A>G ENSP00000509450.1:p.Arg826=
ENST00000688060.1:n.287A>G
ENST00000689832.1:c.2490A>G ENSP00000509084.1:p.Arg830=
ENST00000689994.1:c.1980A>G ENSP00000509156.1:p.Arg660=
ENST00000690543.1:c.2481A>G ENSP00000508831.1:p.Arg827=
ENST00000690917.1:n.2708A>G
ENST00000691361.1:n.1400A>G
ENST00000692301.1:n.1182A>G
ENST00000692783.1:c.2487A>G ENSP00000508733.1:p.Arg829=
ENST00000692991.1:n.2587A>G
ENST00000288135.6:c.2490A>G MANE Select ENSP00000288135.6:p.Arg830=
ENST00000288135.5:c.2490A>G ENSP00000288135.5:p.Arg830=
ENST00000412167.6:c.2478A>G ENSP00000390987.2:p.Arg826=
NM_000222.2:c.2490A>G , LRG_307t1:c.2490A>G NP_000213.1:p.Arg830=
NM_001093772.1:c.2478A>G NP_001087241.1:p.Arg826=
XM_005265740.1:c.2493A>G XP_005265797.1:p.Arg831=
XM_005265741.1:c.2490A>G XP_005265798.1:p.Arg830=
XM_005265742.1:c.2481A>G XP_005265799.1:p.Arg827=
XM_005265742.3:c.2481A>G XP_005265799.1:p.Arg827=
XM_017008178.1:c.2487A>G XP_016863667.1:p.Arg829=
XM_017008179.1:c.2478A>G XP_016863668.1:p.Arg826=
XM_017008180.1:c.2475A>G XP_016863669.1:p.Arg825=
NM_000222.3:c.2490A>G MANE Select NP_000213.1:p.Arg830=
NM_001093772.2:c.2478A>G NP_001087241.1:p.Arg826=
NM_001385284.1:c.2493A>G NP_001372213.1:p.Arg831=
NM_001385285.1:c.2487A>G NP_001372214.1:p.Arg829=
NM_001385286.1:c.2475A>G NP_001372215.1:p.Arg825=
NM_001385288.1:c.2481A>G NP_001372217.1:p.Arg827=
NM_001385290.1:c.2490A>G NP_001372219.1:p.Arg830=
NM_001385292.1:c.2478A>G NP_001372221.1:p.Arg826=