Canonical Allele Identifier: CA2053129411

Gene: KITLG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88560016_88560020delinsAAAGT , CM000674.2:g.88560016_88560020delinsAAAGT	GRCh38
NC_000012.11:g.88953793_88953797delinsAAAGT , CM000674.1:g.88953793_88953797delinsAAAGT	GRCh37
NC_000012.10:g.87477924_87477928delinsAAAGT	NCBI36
NG_012098.1:g.25442_25446delinsACTTT
NG_012098.2:g.25442_25446delinsACTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.16-14155_16-14151delinsACTTT	ENSP00000054216.5:n.16-14155_16-14151delinsACTTT
ENST00000644744.1:c.16-14155_16-14151delinsACTTT MANE Select	ENSP00000495951.1:n.16-14155_16-14151delinsACTTT
ENST00000646633.1:c.*17-14155_*17-14151delinsACTTT	ENSP00000494139.1:n.*17-14155_*17-14151delinsACTTT
ENST00000228280.9:c.16-14155_16-14151delinsACTTT	ENSP00000228280.5:n.16-14155_16-14151delinsACTTT
ENST00000347404.9:c.16-14155_16-14151delinsACTTT	ENSP00000054216.5:n.16-14155_16-14151delinsACTTT
ENST00000357116.4:c.-48+20244_-48+20248delinsACTTT	ENSP00000474021.1:n.-48+20244_-48+20248delinsACTTT
ENST00000552044.1:c.-139+4188_-139+4192delinsACTTT	ENSP00000475042.1:n.-139+4188_-139+4192delinsACTTT
NM_000899.4:c.16-14155_16-14151delinsACTTT	NP_000890.1:n.16-14155_16-14151delinsACTTT
NM_003994.5:c.16-14155_16-14151delinsACTTT	NP_003985.2:n.16-14155_16-14151delinsACTTT
NM_000899.5:c.16-14155_16-14151delinsACTTT MANE Select	NP_000890.1:n.16-14155_16-14151delinsACTTT
NM_003994.6:c.16-14155_16-14151delinsACTTT	NP_003985.2:n.16-14155_16-14151delinsACTTT