Canonical Allele Identifier: CA950237861

Gene: KITLG

Linked Data

• dbSNP Id: rs1871247597
• gnomAD v3: 12-88560051-CG-C
• gnomAD v4: 12-88560051-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88560052del , CM000674.2:g.88560052del	GRCh38
NC_000012.11:g.88953829del , CM000674.1:g.88953829del	GRCh37
NC_000012.10:g.87477960del	NCBI36
NG_012098.1:g.25410del
NG_012098.2:g.25410del

Transcript Alleles

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