Canonical Allele Identifier: CA2620444248

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101761827-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761827A>T , CM000674.2:g.101761827A>T	GRCh38
NC_000012.11:g.102155605A>T , CM000674.1:g.102155605A>T	GRCh37
NC_000012.10:g.100679736A>T	NCBI36
NG_021243.1:g.74041T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2716-64T>A MANE Select	ENSP00000299314.7:n.2716-64T>A
ENST00000299314.11:c.2716-64T>A	ENSP00000299314.7:n.2716-64T>A
NM_024312.4:c.2716-64T>A	NP_077288.2:n.2716-64T>A
XM_006719593.2:c.2716-64T>A	XP_006719656.1:n.2716-64T>A
XM_011538731.1:c.2635-64T>A	XP_011537033.1:n.2635-64T>A
XM_006719593.3:c.2716-64T>A	XP_006719656.1:n.2716-64T>A
XM_011538731.2:c.2635-64T>A	XP_011537033.1:n.2635-64T>A
XM_017019961.1:c.2500-64T>A	XP_016875450.1:n.2500-64T>A
XM_017019962.2:c.1489-64T>A	XP_016875451.1:n.1489-64T>A
NM_024312.5:c.2716-64T>A MANE Select	NP_077288.2:n.2716-64T>A