Canonical Allele Identifier: CA2053131971
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88565642C= , CM000674.2:g.88565642C= GRCh38
NC_000012.11:g.88959419C= , CM000674.1:g.88959419C= GRCh37
NC_000012.10:g.87483550C= NCBI36
NG_012098.1:g.19820G=
NG_012098.2:g.19820G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.15+14622G= ENSP00000054216.5:n.15+14622G=
ENST00000644744.1:c.15+14622G= MANE Select ENSP00000495951.1:n.15+14622G=
ENST00000646633.1:c.*16+14447G= ENSP00000494139.1:n.*16+14447G=
ENST00000228280.9:c.15+14622G= ENSP00000228280.5:n.15+14622G=
ENST00000347404.9:c.15+14622G= ENSP00000054216.5:n.15+14622G=
ENST00000357116.4:c.-48+14622G= ENSP00000474021.1:n.-48+14622G=
ENST00000552044.1:c.-275-1298G= ENSP00000475042.1:n.-275-1298G=
NM_000899.4:c.15+14622G= NP_000890.1:n.15+14622G=
NM_003994.5:c.15+14622G= NP_003985.2:n.15+14622G=
NM_000899.5:c.15+14622G= MANE Select NP_000890.1:n.15+14622G=
NM_003994.6:c.15+14622G= NP_003985.2:n.15+14622G=