Canonical Allele Identifier: CA2053131964
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88565633A= , CM000674.2:g.88565633A= GRCh38
NC_000012.11:g.88959410A= , CM000674.1:g.88959410A= GRCh37
NC_000012.10:g.87483541A= NCBI36
NG_012098.1:g.19829T=
NG_012098.2:g.19829T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.15+14631T= ENSP00000054216.5:n.15+14631T=
ENST00000644744.1:c.15+14631T= MANE Select ENSP00000495951.1:n.15+14631T=
ENST00000646633.1:c.*16+14456T= ENSP00000494139.1:n.*16+14456T=
ENST00000228280.9:c.15+14631T= ENSP00000228280.5:n.15+14631T=
ENST00000347404.9:c.15+14631T= ENSP00000054216.5:n.15+14631T=
ENST00000357116.4:c.-48+14631T= ENSP00000474021.1:n.-48+14631T=
ENST00000552044.1:c.-275-1289T= ENSP00000475042.1:n.-275-1289T=
NM_000899.4:c.15+14631T= NP_000890.1:n.15+14631T=
NM_003994.5:c.15+14631T= NP_003985.2:n.15+14631T=
NM_000899.5:c.15+14631T= MANE Select NP_000890.1:n.15+14631T=
NM_003994.6:c.15+14631T= NP_003985.2:n.15+14631T=