Canonical Allele Identifier: CA950240738

Gene: KITLG

Linked Data

• dbSNP Id: rs1871421002
• gnomAD v3: 12-88565656-A-G
• gnomAD v4: 12-88565656-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88565656A>G , CM000674.2:g.88565656A>G	GRCh38
NC_000012.11:g.88959433A>G , CM000674.1:g.88959433A>G	GRCh37
NC_000012.10:g.87483564A>G	NCBI36
NG_012098.1:g.19806T>C
NG_012098.2:g.19806T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.15+14608T>C	ENSP00000054216.5:n.15+14608T>C
ENST00000644744.1:c.15+14608T>C MANE Select	ENSP00000495951.1:n.15+14608T>C
ENST00000646633.1:c.*16+14433T>C	ENSP00000494139.1:n.*16+14433T>C
ENST00000228280.9:c.15+14608T>C	ENSP00000228280.5:n.15+14608T>C
ENST00000347404.9:c.15+14608T>C	ENSP00000054216.5:n.15+14608T>C
ENST00000357116.4:c.-48+14608T>C	ENSP00000474021.1:n.-48+14608T>C
ENST00000552044.1:c.-275-1312T>C	ENSP00000475042.1:n.-275-1312T>C
NM_000899.4:c.15+14608T>C	NP_000890.1:n.15+14608T>C
NM_003994.5:c.15+14608T>C	NP_003985.2:n.15+14608T>C
NM_000899.5:c.15+14608T>C MANE Select	NP_000890.1:n.15+14608T>C
NM_003994.6:c.15+14608T>C	NP_003985.2:n.15+14608T>C