Canonical Allele Identifier: CA386296506

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155535C>A (hg19) ; chr12:g.101761757C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761757C>A , CM000674.2:g.101761757C>A	GRCh38
NC_000012.11:g.102155535C>A , CM000674.1:g.102155535C>A	GRCh37
NC_000012.10:g.100679666C>A	NCBI36
NG_021243.1:g.74111G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2722G>T MANE Select	ENSP00000299314.7:p.Glu908Ter
ENST00000299314.11:c.2722G>T	ENSP00000299314.7:p.Glu908Ter
NM_024312.4:c.2722G>T	NP_077288.2:p.Glu908Ter
XM_006719593.2:c.2722G>T	XP_006719656.1:p.Glu908Ter
XM_011538731.1:c.2641G>T	XP_011537033.1:p.Glu881Ter
XM_006719593.3:c.2722G>T	XP_006719656.1:p.Glu908Ter
XM_011538731.2:c.2641G>T	XP_011537033.1:p.Glu881Ter
XM_017019961.1:c.2506G>T	XP_016875450.1:p.Glu836Ter
XM_017019962.2:c.1495G>T	XP_016875451.1:p.Glu499Ter
NM_024312.5:c.2722G>T MANE Select	NP_077288.2:p.Glu908Ter