Canonical Allele Identifier: CA2053132004
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88565723T= , CM000674.2:g.88565723T= GRCh38
NC_000012.11:g.88959500T= , CM000674.1:g.88959500T= GRCh37
NC_000012.10:g.87483631T= NCBI36
NG_012098.1:g.19739A=
NG_012098.2:g.19739A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.15+14541A= ENSP00000054216.5:n.15+14541A=
ENST00000644744.1:c.15+14541A= MANE Select ENSP00000495951.1:n.15+14541A=
ENST00000646633.1:c.*16+14366A= ENSP00000494139.1:n.*16+14366A=
ENST00000228280.9:c.15+14541A= ENSP00000228280.5:n.15+14541A=
ENST00000347404.9:c.15+14541A= ENSP00000054216.5:n.15+14541A=
ENST00000357116.4:c.-48+14541A= ENSP00000474021.1:n.-48+14541A=
ENST00000552044.1:c.-275-1379A= ENSP00000475042.1:n.-275-1379A=
NM_000899.4:c.15+14541A= NP_000890.1:n.15+14541A=
NM_003994.5:c.15+14541A= NP_003985.2:n.15+14541A=
NM_000899.5:c.15+14541A= MANE Select NP_000890.1:n.15+14541A=
NM_003994.6:c.15+14541A= NP_003985.2:n.15+14541A=