Canonical Allele Identifier: CA481136708

Gene: KITLG

Linked Data

• gnomAD v4: 12-88545797-G-T
• MyVariant Identifiers: chr12:g.88939574G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88545797G>T , CM000674.2:g.88545797G>T	GRCh38
NC_000012.11:g.88939574G>T , CM000674.1:g.88939574G>T	GRCh37
NC_000012.10:g.87463705G>T	NCBI36
NG_012098.1:g.39665C>A
NG_012098.2:g.39665C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.84C>A	ENSP00000054216.5:p.Ile28=
ENST00000644744.1:c.84C>A MANE Select	ENSP00000495951.1:p.Ile28=
ENST00000646633.1:c.*85C>A	ENSP00000494139.1:n.*85C>A
ENST00000228280.9:c.84C>A	ENSP00000228280.5:p.Ile28=
ENST00000347404.9:c.84C>A	ENSP00000054216.5:p.Ile28=
ENST00000357116.4:c.-48+34467C>A	ENSP00000474021.1:n.-48+34467C>A
ENST00000552044.1:c.-70C>A	ENSP00000475042.1:n.-70C>A
NM_000899.4:c.84C>A	NP_000890.1:p.Ile28=
NM_003994.5:c.84C>A	NP_003985.2:p.Ile28=
NM_000899.5:c.84C>A MANE Select	NP_000890.1:p.Ile28=
NM_003994.6:c.84C>A	NP_003985.2:p.Ile28=