Canonical Allele Identifier: CA481327914

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102190505A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796727A>T , CM000674.2:g.101796727A>T	GRCh38
NC_000012.11:g.102190505A>T , CM000674.1:g.102190505A>T	GRCh37
NC_000012.10:g.100714636A>T	NCBI36
NG_021243.1:g.39141T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.153T>A MANE Select	ENSP00000299314.7:p.Val51=
ENST00000647144.1:n.273T>A
ENST00000299314.11:c.153T>A	ENSP00000299314.7:p.Val51=
ENST00000392919.4:c.153T>A	ENSP00000376651.4:p.Val51=
ENST00000549165.1:c.153T>A	ENSP00000450413.1:p.Val51=
ENST00000549940.5:c.153T>A	ENSP00000449150.1:p.Val51=
NM_024312.4:c.153T>A	NP_077288.2:p.Val51=
XM_006719593.2:c.153T>A	XP_006719656.1:p.Val51=
XM_011538731.1:c.72T>A	XP_011537033.1:p.Val24=
XM_006719593.3:c.153T>A	XP_006719656.1:p.Val51=
XM_011538731.2:c.72T>A	XP_011537033.1:p.Val24=
XM_017019961.1:c.-64T>A	XP_016875450.1:n.-64T>A
XM_017019962.2:c.-1198T>A	XP_016875451.1:n.-1198T>A
NM_024312.5:c.153T>A MANE Select	NP_077288.2:p.Val51=