Canonical Allele Identifier: CA2053129429

Gene: KITLG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88560051_88560052delinsCG , CM000674.2:g.88560051_88560052delinsCG	GRCh38
NC_000012.11:g.88953828_88953829delinsCG , CM000674.1:g.88953828_88953829delinsCG	GRCh37
NC_000012.10:g.87477959_87477960delinsCG	NCBI36
NG_012098.1:g.25410_25411delinsCG
NG_012098.2:g.25410_25411delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.16-14187_16-14186delinsCG	ENSP00000054216.5:n.16-14187_16-14186delinsCG
ENST00000644744.1:c.16-14187_16-14186delinsCG MANE Select	ENSP00000495951.1:n.16-14187_16-14186delinsCG
ENST00000646633.1:c.*17-14187_*17-14186delinsCG	ENSP00000494139.1:n.*17-14187_*17-14186delinsCG
ENST00000228280.9:c.16-14187_16-14186delinsCG	ENSP00000228280.5:n.16-14187_16-14186delinsCG
ENST00000347404.9:c.16-14187_16-14186delinsCG	ENSP00000054216.5:n.16-14187_16-14186delinsCG
ENST00000357116.4:c.-48+20212_-48+20213delinsCG	ENSP00000474021.1:n.-48+20212_-48+20213delinsCG
ENST00000552044.1:c.-139+4156_-139+4157delinsCG	ENSP00000475042.1:n.-139+4156_-139+4157delinsCG
NM_000899.4:c.16-14187_16-14186delinsCG	NP_000890.1:n.16-14187_16-14186delinsCG
NM_003994.5:c.16-14187_16-14186delinsCG	NP_003985.2:n.16-14187_16-14186delinsCG
NM_000899.5:c.16-14187_16-14186delinsCG MANE Select	NP_000890.1:n.16-14187_16-14186delinsCG
NM_003994.6:c.16-14187_16-14186delinsCG	NP_003985.2:n.16-14187_16-14186delinsCG