Canonical Allele Identifier: CA386123066

Gene: KITLG

Linked Data

• MyVariant Identifiers: chr12:g.88939590A>C (hg19) ; chr12:g.88545813A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88545813A>C , CM000674.2:g.88545813A>C	GRCh38
NC_000012.11:g.88939590A>C , CM000674.1:g.88939590A>C	GRCh37
NC_000012.10:g.87463721A>C	NCBI36
NG_012098.1:g.39649T>G
NG_012098.2:g.39649T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.68T>G	ENSP00000054216.5:p.Val23Gly
ENST00000644744.1:c.68T>G MANE Select	ENSP00000495951.1:p.Val23Gly
ENST00000646633.1:c.*69T>G	ENSP00000494139.1:n.*69T>G
ENST00000228280.9:c.68T>G	ENSP00000228280.5:p.Val23Gly
ENST00000347404.9:c.68T>G	ENSP00000054216.5:p.Val23Gly
ENST00000357116.4:c.-48+34451T>G	ENSP00000474021.1:n.-48+34451T>G
ENST00000552044.1:c.-86T>G	ENSP00000475042.1:n.-86T>G
NM_000899.4:c.68T>G	NP_000890.1:p.Val23Gly
NM_003994.5:c.68T>G	NP_003985.2:p.Val23Gly
NM_000899.5:c.68T>G MANE Select	NP_000890.1:p.Val23Gly
NM_003994.6:c.68T>G	NP_003985.2:p.Val23Gly