Canonical Allele Identifier: CA481136632

Gene: KITLG

Linked Data

• MyVariant Identifiers: chr12:g.88926218C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532441C>T , CM000674.2:g.88532441C>T	GRCh38
NC_000012.11:g.88926218C>T , CM000674.1:g.88926218C>T	GRCh37
NC_000012.10:g.87450349C>T	NCBI36
NG_012098.1:g.53021G>A
NG_012098.2:g.53021G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192G>A	ENSP00000054216.5:p.Leu64=
ENST00000644744.1:c.192G>A MANE Select	ENSP00000495951.1:p.Leu64=
ENST00000646633.1:c.*193G>A	ENSP00000494139.1:n.*193G>A
ENST00000228280.9:c.192G>A	ENSP00000228280.5:p.Leu64=
ENST00000347404.9:c.192G>A	ENSP00000054216.5:p.Leu64=
ENST00000357116.4:c.-47-25304G>A	ENSP00000474021.1:n.-47-25304G>A
ENST00000378535.4:n.135G>A
ENST00000552044.1:c.39G>A	ENSP00000475042.1:p.Leu13=
NM_000899.4:c.192G>A	NP_000890.1:p.Leu64=
NM_003994.5:c.192G>A	NP_003985.2:p.Leu64=
NM_000899.5:c.192G>A MANE Select	NP_000890.1:p.Leu64=
NM_003994.6:c.192G>A	NP_003985.2:p.Leu64=