Canonical Allele Identifier: CA2620120763

Gene: KITLG

Linked Data

• gnomAD v4: 12-88545703-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88545703A>G , CM000674.2:g.88545703A>G	GRCh38
NC_000012.11:g.88939480A>G , CM000674.1:g.88939480A>G	GRCh37
NC_000012.10:g.87463611A>G	NCBI36
NG_012098.1:g.39759T>C
NG_012098.2:g.39759T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.129+49T>C	ENSP00000054216.5:n.129+49T>C
ENST00000644744.1:c.129+49T>C MANE Select	ENSP00000495951.1:n.129+49T>C
ENST00000646633.1:c.*130+49T>C	ENSP00000494139.1:n.*130+49T>C
ENST00000228280.9:c.129+49T>C	ENSP00000228280.5:n.129+49T>C
ENST00000347404.9:c.129+49T>C	ENSP00000054216.5:n.129+49T>C
ENST00000357116.4:c.-48+34561T>C	ENSP00000474021.1:n.-48+34561T>C
ENST00000552044.1:c.-25+49T>C	ENSP00000475042.1:n.-25+49T>C
NM_000899.4:c.129+49T>C	NP_000890.1:n.129+49T>C
NM_003994.5:c.129+49T>C	NP_003985.2:n.129+49T>C
NM_000899.5:c.129+49T>C MANE Select	NP_000890.1:n.129+49T>C
NM_003994.6:c.129+49T>C	NP_003985.2:n.129+49T>C