Canonical Allele Identifier: CA2580101947

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727324_54727455del , CM000666.2:g.54727324_54727455del	GRCh38
NC_000004.11:g.55593490_55593621del , CM000666.1:g.55593490_55593621del	GRCh37
NC_000004.10:g.55288247_55288378del	NCBI36
NG_007456.1:g.74330_74461del , LRG_307:g.74330_74461del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1638_1678del
ENST00000685269.1:n.1725_1765del
ENST00000686011.1:c.1635_1675del
ENST00000687109.1:c.1650_1690del
ENST00000687208.1:n.2062_2102del
ENST00000687246.1:c.1635_1675del
ENST00000687265.1:n.1805_1845del
ENST00000687295.1:c.1635_1675del
ENST00000689832.1:c.1650_1690del
ENST00000689994.1:c.1137_1177del
ENST00000690543.1:c.1638_1678del
ENST00000690917.1:n.1865_1905del
ENST00000691361.1:n.557_597del
ENST00000692783.1:c.1647_1687del
ENST00000692991.1:n.1744_1784del
ENST00000288135.6:c.1647_1687del
ENST00000288135.5:c.1647_1687del
ENST00000412167.6:c.1635_1675del
NM_000222.2:c.1647_1687del , LRG_307t1:c.1647_1687del
NM_001093772.1:c.1635_1675del
XM_005265740.1:c.1650_1690del
XM_005265741.1:c.1650_1690del
XM_005265742.1:c.1638_1678del
XM_005265742.3:c.1638_1678del
XM_017008178.1:c.1647_1687del
XM_017008179.1:c.1638_1678del
XM_017008180.1:c.1635_1675del
NM_000222.3:c.1647_1687del
NM_001093772.2:c.1635_1675del
NM_001385284.1:c.1650_1690del
NM_001385285.1:c.1647_1687del
NM_001385286.1:c.1635_1675del
NM_001385288.1:c.1638_1678del
NM_001385290.1:c.1650_1690del
NM_001385292.1:c.1638_1678del