Canonical Allele Identifier: CA606614654

Gene: KITLG

Linked Data

• dbSNP Id: rs1449977965
• gnomAD v2: 12-88953793-AAAGT-A
• MyVariant Identifiers: chr12:g.88953794_88953797del (hg19) ; chr12:g.88560017_88560020del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88560020_88560023del , CM000674.2:g.88560020_88560023del	GRCh38
NC_000012.11:g.88953797_88953800del , CM000674.1:g.88953797_88953800del	GRCh37
NC_000012.10:g.87477928_87477931del	NCBI36
NG_012098.1:g.25442_25445del
NG_012098.2:g.25442_25445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.16-14155_16-14152del	ENSP00000054216.5:n.16-14155_16-14152del
ENST00000644744.1:c.16-14155_16-14152del MANE Select	ENSP00000495951.1:n.16-14155_16-14152del
ENST00000646633.1:c.*17-14155_*17-14152del	ENSP00000494139.1:n.*17-14155_*17-14152del
ENST00000228280.9:c.16-14155_16-14152del	ENSP00000228280.5:n.16-14155_16-14152del
ENST00000347404.9:c.16-14155_16-14152del	ENSP00000054216.5:n.16-14155_16-14152del
ENST00000357116.4:c.-48+20244_-48+20247del	ENSP00000474021.1:n.-48+20244_-48+20247del
ENST00000552044.1:c.-139+4188_-139+4191del	ENSP00000475042.1:n.-139+4188_-139+4191del
NM_000899.4:c.16-14155_16-14152del	NP_000890.1:n.16-14155_16-14152del
NM_003994.5:c.16-14155_16-14152del	NP_003985.2:n.16-14155_16-14152del
NM_000899.5:c.16-14155_16-14152del MANE Select	NP_000890.1:n.16-14155_16-14152del
NM_003994.6:c.16-14155_16-14152del	NP_003985.2:n.16-14155_16-14152del