Canonical Allele Identifier: CA386301745

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101768048-C-T
• MyVariant Identifiers: chr12:g.102161826C>T (hg19) ; chr12:g.101768048C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768048C>T , CM000674.2:g.101768048C>T	GRCh38
NC_000012.11:g.102161826C>T , CM000674.1:g.102161826C>T	GRCh37
NC_000012.10:g.100685957C>T	NCBI36
NG_021243.1:g.67820G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1397G>A MANE Select	ENSP00000299314.7:p.Gly466Glu
ENST00000299314.11:c.1397G>A	ENSP00000299314.7:p.Gly466Glu
ENST00000549940.5:c.1397G>A	ENSP00000449150.1:p.Gly466Glu
ENST00000552009.1:n.56G>A
NM_024312.4:c.1397G>A	NP_077288.2:p.Gly466Glu
XM_006719593.2:c.1397G>A	XP_006719656.1:p.Gly466Glu
XM_011538731.1:c.1316G>A	XP_011537033.1:p.Gly439Glu
XM_006719593.3:c.1397G>A	XP_006719656.1:p.Gly466Glu
XM_011538731.2:c.1316G>A	XP_011537033.1:p.Gly439Glu
XM_017019961.1:c.1181G>A	XP_016875450.1:p.Gly394Glu
XM_017019962.2:c.170G>A	XP_016875451.1:p.Gly57Glu
NM_024312.5:c.1397G>A MANE Select	NP_077288.2:p.Gly466Glu