Canonical Allele Identifier: CA481576811

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155461T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761683T>C , CM000674.2:g.101761683T>C	GRCh38
NC_000012.11:g.102155461T>C , CM000674.1:g.102155461T>C	GRCh37
NC_000012.10:g.100679592T>C	NCBI36
NG_021243.1:g.74185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2796A>G MANE Select	ENSP00000299314.7:p.Ala932=
ENST00000299314.11:c.2796A>G	ENSP00000299314.7:p.Ala932=
NM_024312.4:c.2796A>G	NP_077288.2:p.Ala932=
XM_006719593.2:c.2796A>G	XP_006719656.1:p.Ala932=
XM_011538731.1:c.2715A>G	XP_011537033.1:p.Ala905=
XM_006719593.3:c.2796A>G	XP_006719656.1:p.Ala932=
XM_011538731.2:c.2715A>G	XP_011537033.1:p.Ala905=
XM_017019961.1:c.2580A>G	XP_016875450.1:p.Ala860=
XM_017019962.2:c.1569A>G	XP_016875451.1:p.Ala523=
NM_024312.5:c.2796A>G MANE Select	NP_077288.2:p.Ala932=