Canonical Allele Identifier: CA2053117181
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88532285_88532286delinsGA , CM000674.2:g.88532285_88532286delinsGA GRCh38
NC_000012.11:g.88926062_88926063delinsGA , CM000674.1:g.88926062_88926063delinsGA GRCh37
NC_000012.10:g.87450193_87450194delinsGA NCBI36
NG_012098.1:g.53176_53177delinsTC
NG_012098.2:g.53176_53177delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.192+155_192+156delinsTC ENSP00000054216.5:n.192+155_192+156delinsTC
ENST00000644744.1:c.192+155_192+156delinsTC MANE Select ENSP00000495951.1:n.192+155_192+156delinsTC
ENST00000646633.1:c.*193+155_*193+156delinsTC ENSP00000494139.1:n.*193+155_*193+156delinsTC
ENST00000228280.9:c.192+155_192+156delinsTC ENSP00000228280.5:n.192+155_192+156delinsTC
ENST00000347404.9:c.192+155_192+156delinsTC ENSP00000054216.5:n.192+155_192+156delinsTC
ENST00000357116.4:c.-47-25149_-47-25148delinsTC ENSP00000474021.1:n.-47-25149_-47-25148delinsTC
ENST00000378535.4:n.135+155_135+156delinsTC
ENST00000552044.1:c.39+155_39+156delinsTC ENSP00000475042.1:n.39+155_39+156delinsTC
NM_000899.4:c.192+155_192+156delinsTC NP_000890.1:n.192+155_192+156delinsTC
NM_003994.5:c.192+155_192+156delinsTC NP_003985.2:n.192+155_192+156delinsTC
NM_000899.5:c.192+155_192+156delinsTC MANE Select NP_000890.1:n.192+155_192+156delinsTC
NM_003994.6:c.192+155_192+156delinsTC NP_003985.2:n.192+155_192+156delinsTC