Canonical Allele Identifier: CA356907424
Gene: KIT HGNC NCBI

Linked Data

dbSNP Id: rs1722299442

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727420C>A , CM000666.2:g.54727420C>A GRCh38
NC_000004.11:g.55593586C>A , CM000666.1:g.55593586C>A GRCh37
NC_000004.10:g.55288343C>A NCBI36
NG_007456.1:g.74426C>A , LRG_307:g.74426C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1643C>A ENSP00000390987.3:p.Pro548His
ENST00000685269.1:n.1730C>A
ENST00000686011.1:c.1640C>A ENSP00000509704.1:p.Pro547His
ENST00000687109.1:c.1655C>A ENSP00000509371.1:p.Pro552His
ENST00000687208.1:n.2067C>A
ENST00000687246.1:c.1640C>A ENSP00000509114.1:p.Pro547His
ENST00000687265.1:n.1810C>A
ENST00000687295.1:c.1640C>A ENSP00000509450.1:p.Pro547His
ENST00000689832.1:c.1655C>A ENSP00000509084.1:p.Pro552His
ENST00000689994.1:c.1142C>A ENSP00000509156.1:p.Pro381His
ENST00000690543.1:c.1643C>A ENSP00000508831.1:p.Pro548His
ENST00000690917.1:n.1870C>A
ENST00000691361.1:n.562C>A
ENST00000692783.1:c.1652C>A ENSP00000508733.1:p.Pro551His
ENST00000692991.1:n.1749C>A
ENST00000288135.6:c.1652C>A MANE Select ENSP00000288135.6:p.Pro551His
ENST00000288135.5:c.1652C>A ENSP00000288135.5:p.Pro551His
ENST00000412167.6:c.1640C>A ENSP00000390987.2:p.Pro547His
NM_000222.2:c.1652C>A , LRG_307t1:c.1652C>A NP_000213.1:p.Pro551His
NM_001093772.1:c.1640C>A NP_001087241.1:p.Pro547His
XM_005265740.1:c.1655C>A XP_005265797.1:p.Pro552His
XM_005265741.1:c.1655C>A XP_005265798.1:p.Pro552His
XM_005265742.1:c.1643C>A XP_005265799.1:p.Pro548His
XM_005265742.3:c.1643C>A XP_005265799.1:p.Pro548His
XM_017008178.1:c.1652C>A XP_016863667.1:p.Pro551His
XM_017008179.1:c.1643C>A XP_016863668.1:p.Pro548His
XM_017008180.1:c.1640C>A XP_016863669.1:p.Pro547His
NM_000222.3:c.1652C>A MANE Select NP_000213.1:p.Pro551His
NM_001093772.2:c.1640C>A NP_001087241.1:p.Pro547His
NM_001385284.1:c.1655C>A NP_001372213.1:p.Pro552His
NM_001385285.1:c.1652C>A NP_001372214.1:p.Pro551His
NM_001385286.1:c.1640C>A NP_001372215.1:p.Pro547His
NM_001385288.1:c.1643C>A NP_001372217.1:p.Pro548His
NM_001385290.1:c.1655C>A NP_001372219.1:p.Pro552His
NM_001385292.1:c.1643C>A NP_001372221.1:p.Pro548His