Canonical Allele Identifier: CA386122880

Gene: KITLG

Linked Data

• gnomAD v4: 12-88532483-G-T
• MyVariant Identifiers: chr12:g.88926260G>T (hg19) ; chr12:g.88532483G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532483G>T , CM000674.2:g.88532483G>T	GRCh38
NC_000012.11:g.88926260G>T , CM000674.1:g.88926260G>T	GRCh37
NC_000012.10:g.87450391G>T	NCBI36
NG_012098.1:g.52979C>A
NG_012098.2:g.52979C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.150C>A	ENSP00000054216.5:p.Asp50Glu
ENST00000644744.1:c.150C>A MANE Select	ENSP00000495951.1:p.Asp50Glu
ENST00000646633.1:c.*151C>A	ENSP00000494139.1:n.*151C>A
ENST00000228280.9:c.150C>A	ENSP00000228280.5:p.Asp50Glu
ENST00000347404.9:c.150C>A	ENSP00000054216.5:p.Asp50Glu
ENST00000357116.4:c.-47-25346C>A	ENSP00000474021.1:n.-47-25346C>A
ENST00000378535.4:n.93C>A
ENST00000552044.1:c.-4C>A	ENSP00000475042.1:n.-4C>A
NM_000899.4:c.150C>A	NP_000890.1:p.Asp50Glu
NM_003994.5:c.150C>A	NP_003985.2:p.Asp50Glu
NM_000899.5:c.150C>A MANE Select	NP_000890.1:p.Asp50Glu
NM_003994.6:c.150C>A	NP_003985.2:p.Asp50Glu