Canonical Allele Identifier: CA1458747218
Gene: KIT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54736577A= , CM000666.2:g.54736577A= GRCh38
NC_000004.11:g.55602743A= , CM000666.1:g.55602743A= GRCh37
NC_000004.10:g.55297500A= NCBI36
NG_007456.1:g.83583A= , LRG_307:g.83583A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.2552A= ENSP00000390987.3:p.Tyr851=
ENST00000684818.1:n.1256A=
ENST00000685269.1:n.2642A=
ENST00000686011.1:c.2549A= ENSP00000509704.1:p.Tyr850=
ENST00000687109.1:c.2567A= ENSP00000509371.1:p.Tyr856=
ENST00000687208.1:n.2976A=
ENST00000687246.1:c.2429A= ENSP00000509114.1:p.Tyr810=
ENST00000687265.1:n.2722A=
ENST00000687295.1:c.2552A= ENSP00000509450.1:p.Tyr851=
ENST00000688060.1:n.361A=
ENST00000689832.1:c.2564A= ENSP00000509084.1:p.Tyr855=
ENST00000689994.1:c.2054A= ENSP00000509156.1:p.Tyr685=
ENST00000690543.1:c.2555A= ENSP00000508831.1:p.Tyr852=
ENST00000690917.1:n.2782A=
ENST00000691361.1:n.1474A=
ENST00000692301.1:n.1256A=
ENST00000692783.1:c.2561A= ENSP00000508733.1:p.Tyr854=
ENST00000692991.1:n.2661A=
ENST00000288135.6:c.2564A= MANE Select ENSP00000288135.6:p.Tyr855=
ENST00000288135.5:c.2564A= ENSP00000288135.5:p.Tyr855=
ENST00000412167.6:c.2552A= ENSP00000390987.2:p.Tyr851=
NM_000222.2:c.2564A= , LRG_307t1:c.2564A= NP_000213.1:p.Tyr855=
NM_001093772.1:c.2552A= NP_001087241.1:p.Tyr851=
XM_005265740.1:c.2567A= XP_005265797.1:p.Tyr856=
XM_005265741.1:c.2564A= XP_005265798.1:p.Tyr855=
XM_005265742.1:c.2555A= XP_005265799.1:p.Tyr852=
XM_005265742.3:c.2555A= XP_005265799.1:p.Tyr852=
XM_017008178.1:c.2561A= XP_016863667.1:p.Tyr854=
XM_017008179.1:c.2552A= XP_016863668.1:p.Tyr851=
XM_017008180.1:c.2549A= XP_016863669.1:p.Tyr850=
NM_000222.3:c.2564A= MANE Select NP_000213.1:p.Tyr855=
NM_001093772.2:c.2552A= NP_001087241.1:p.Tyr851=
NM_001385284.1:c.2567A= NP_001372213.1:p.Tyr856=
NM_001385285.1:c.2561A= NP_001372214.1:p.Tyr854=
NM_001385286.1:c.2549A= NP_001372215.1:p.Tyr850=
NM_001385288.1:c.2555A= NP_001372217.1:p.Tyr852=
NM_001385290.1:c.2564A= NP_001372219.1:p.Tyr855=
NM_001385292.1:c.2552A= NP_001372221.1:p.Tyr851=