Canonical Allele Identifier: CA2053119517
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88545696_88545697delinsAG , CM000674.2:g.88545696_88545697delinsAG GRCh38
NC_000012.11:g.88939473_88939474delinsAG , CM000674.1:g.88939473_88939474delinsAG GRCh37
NC_000012.10:g.87463604_87463605delinsAG NCBI36
NG_012098.1:g.39765_39766delinsCT
NG_012098.2:g.39765_39766delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000347404.10:c.129+55_129+56delinsCT ENSP00000054216.5:n.129+55_129+56delinsCT...
ENST00000644744.1:c.129+55_129+56delinsCT MANE Select ENSP00000495951.1:n.129+55_129+56delinsCT...
ENST00000646633.1:c.*130+55_*130+56delinsCT ENSP00000494139.1:n.*130+55_*130+56delins...
ENST00000228280.9:c.129+55_129+56delinsCT ENSP00000228280.5:n.129+55_129+56delinsCT...
ENST00000347404.9:c.129+55_129+56delinsCT ENSP00000054216.5:n.129+55_129+56delinsCT...
ENST00000357116.4:c.-48+34567_-48+34568delinsCT ENSP00000474021.1:n.-48+34567_-48+34568de...
ENST00000552044.1:c.-25+55_-25+56delinsCT ENSP00000475042.1:n.-25+55_-25+56delinsCT...
NM_000899.4:c.129+55_129+56delinsCT NP_000890.1:n.129+55_129+56delinsCT
NM_003994.5:c.129+55_129+56delinsCT NP_003985.2:n.129+55_129+56delinsCT
NM_000899.5:c.129+55_129+56delinsCT MANE Select NP_000890.1:n.129+55_129+56delinsCT
NM_003994.6:c.129+55_129+56delinsCT NP_003985.2:n.129+55_129+56delinsCT