Canonical Allele Identifier: CA2053131973

Gene: KITLG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88565646_88565647delinsCA , CM000674.2:g.88565646_88565647delinsCA	GRCh38
NC_000012.11:g.88959423_88959424delinsCA , CM000674.1:g.88959423_88959424delinsCA	GRCh37
NC_000012.10:g.87483554_87483555delinsCA	NCBI36
NG_012098.1:g.19815_19816delinsTG
NG_012098.2:g.19815_19816delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.15+14617_15+14618delinsTG	ENSP00000054216.5:n.15+14617_15+14618delinsTG
ENST00000644744.1:c.15+14617_15+14618delinsTG MANE Select	ENSP00000495951.1:n.15+14617_15+14618delinsTG
ENST00000646633.1:c.*16+14442_*16+14443delinsTG	ENSP00000494139.1:n.*16+14442_*16+14443delinsTG
ENST00000228280.9:c.15+14617_15+14618delinsTG	ENSP00000228280.5:n.15+14617_15+14618delinsTG
ENST00000347404.9:c.15+14617_15+14618delinsTG	ENSP00000054216.5:n.15+14617_15+14618delinsTG
ENST00000357116.4:c.-48+14617_-48+14618delinsTG	ENSP00000474021.1:n.-48+14617_-48+14618delinsTG
ENST00000552044.1:c.-275-1303_-275-1302delinsTG	ENSP00000475042.1:n.-275-1303_-275-1302delinsTG
NM_000899.4:c.15+14617_15+14618delinsTG	NP_000890.1:n.15+14617_15+14618delinsTG
NM_003994.5:c.15+14617_15+14618delinsTG	NP_003985.2:n.15+14617_15+14618delinsTG
NM_000899.5:c.15+14617_15+14618delinsTG MANE Select	NP_000890.1:n.15+14617_15+14618delinsTG
NM_003994.6:c.15+14617_15+14618delinsTG	NP_003985.2:n.15+14617_15+14618delinsTG