Canonical Allele Identifier: CA2053131949

Gene: KITLG

Linked Data

• dbSNP Id: rs1871418631

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88565605C>T , CM000674.2:g.88565605C>T	GRCh38
NC_000012.11:g.88959382C>T , CM000674.1:g.88959382C>T	GRCh37
NC_000012.10:g.87483513C>T	NCBI36
NG_012098.1:g.19857G>A
NG_012098.2:g.19857G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.15+14659G>A	ENSP00000054216.5:n.15+14659G>A
ENST00000644744.1:c.15+14659G>A MANE Select	ENSP00000495951.1:n.15+14659G>A
ENST00000646633.1:c.*16+14484G>A	ENSP00000494139.1:n.*16+14484G>A
ENST00000228280.9:c.15+14659G>A	ENSP00000228280.5:n.15+14659G>A
ENST00000347404.9:c.15+14659G>A	ENSP00000054216.5:n.15+14659G>A
ENST00000357116.4:c.-48+14659G>A	ENSP00000474021.1:n.-48+14659G>A
ENST00000552044.1:c.-275-1261G>A	ENSP00000475042.1:n.-275-1261G>A
NM_000899.4:c.15+14659G>A	NP_000890.1:n.15+14659G>A
NM_003994.5:c.15+14659G>A	NP_003985.2:n.15+14659G>A
NM_000899.5:c.15+14659G>A MANE Select	NP_000890.1:n.15+14659G>A
NM_003994.6:c.15+14659G>A	NP_003985.2:n.15+14659G>A