Canonical Allele Identifier: CA481319177

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102158025G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101764247G>C , CM000674.2:g.101764247G>C	GRCh38
NC_000012.11:g.102158025G>C , CM000674.1:g.102158025G>C	GRCh37
NC_000012.10:g.100682156G>C	NCBI36
NG_021243.1:g.71621C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2670C>G MANE Select	ENSP00000299314.7:p.Gly890=
ENST00000299314.11:c.2670C>G	ENSP00000299314.7:p.Gly890=
NM_024312.4:c.2670C>G	NP_077288.2:p.Gly890=
XM_006719593.2:c.2670C>G	XP_006719656.1:p.Gly890=
XM_011538731.1:c.2589C>G	XP_011537033.1:p.Gly863=
XM_006719593.3:c.2670C>G	XP_006719656.1:p.Gly890=
XM_011538731.2:c.2589C>G	XP_011537033.1:p.Gly863=
XM_017019961.1:c.2454C>G	XP_016875450.1:p.Gly818=
XM_017019962.2:c.1443C>G	XP_016875451.1:p.Gly481=
NM_024312.5:c.2670C>G MANE Select	NP_077288.2:p.Gly890=