Canonical Allele Identifier: CA2620119529

Gene: KITLG

Linked Data

• gnomAD v4: 12-88532405-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532405C>G , CM000674.2:g.88532405C>G	GRCh38
NC_000012.11:g.88926182C>G , CM000674.1:g.88926182C>G	GRCh37
NC_000012.10:g.87450313C>G	NCBI36
NG_012098.1:g.53057G>C
NG_012098.2:g.53057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+36G>C	ENSP00000054216.5:n.192+36G>C
ENST00000644744.1:c.192+36G>C MANE Select	ENSP00000495951.1:n.192+36G>C
ENST00000646633.1:c.*193+36G>C	ENSP00000494139.1:n.*193+36G>C
ENST00000228280.9:c.192+36G>C	ENSP00000228280.5:n.192+36G>C
ENST00000347404.9:c.192+36G>C	ENSP00000054216.5:n.192+36G>C
ENST00000357116.4:c.-47-25268G>C	ENSP00000474021.1:n.-47-25268G>C
ENST00000378535.4:n.135+36G>C
ENST00000552044.1:c.39+36G>C	ENSP00000475042.1:n.39+36G>C
NM_000899.4:c.192+36G>C	NP_000890.1:n.192+36G>C
NM_003994.5:c.192+36G>C	NP_003985.2:n.192+36G>C
NM_000899.5:c.192+36G>C MANE Select	NP_000890.1:n.192+36G>C
NM_003994.6:c.192+36G>C	NP_003985.2:n.192+36G>C