Canonical Allele Identifier: CA2053117175

Gene: KITLG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532277_88532279delinsAAG , CM000674.2:g.88532277_88532279delinsAAG	GRCh38
NC_000012.11:g.88926054_88926056delinsAAG , CM000674.1:g.88926054_88926056delinsAAG	GRCh37
NC_000012.10:g.87450185_87450187delinsAAG	NCBI36
NG_012098.1:g.53183_53185delinsCTT
NG_012098.2:g.53183_53185delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+162_192+164delinsCTT	ENSP00000054216.5:n.192+162_192+164delinsCTT
ENST00000644744.1:c.192+162_192+164delinsCTT MANE Select	ENSP00000495951.1:n.192+162_192+164delinsCTT
ENST00000646633.1:c.*193+162_*193+164delinsCTT	ENSP00000494139.1:n.*193+162_*193+164delinsCTT
ENST00000228280.9:c.192+162_192+164delinsCTT	ENSP00000228280.5:n.192+162_192+164delinsCTT
ENST00000347404.9:c.192+162_192+164delinsCTT	ENSP00000054216.5:n.192+162_192+164delinsCTT
ENST00000357116.4:c.-47-25142_-47-25140delinsCTT	ENSP00000474021.1:n.-47-25142_-47-25140delinsCTT
ENST00000378535.4:n.135+162_135+164delinsCTT
ENST00000552044.1:c.39+162_39+164delinsCTT	ENSP00000475042.1:n.39+162_39+164delinsCTT
NM_000899.4:c.192+162_192+164delinsCTT	NP_000890.1:n.192+162_192+164delinsCTT
NM_003994.5:c.192+162_192+164delinsCTT	NP_003985.2:n.192+162_192+164delinsCTT
NM_000899.5:c.192+162_192+164delinsCTT MANE Select	NP_000890.1:n.192+162_192+164delinsCTT
NM_003994.6:c.192+162_192+164delinsCTT	NP_003985.2:n.192+162_192+164delinsCTT