Canonical Allele Identifier: CA386294753

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101760089-C-A
• MyVariant Identifiers: chr12:g.102153867C>A (hg19) ; chr12:g.101760089C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760089C>A , CM000674.2:g.101760089C>A	GRCh38
NC_000012.11:g.102153867C>A , CM000674.1:g.102153867C>A	GRCh37
NC_000012.10:g.100677998C>A	NCBI36
NG_021243.1:g.75779G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3190G>T MANE Select	ENSP00000299314.7:p.Asp1064Tyr
ENST00000299314.11:c.3190G>T	ENSP00000299314.7:p.Asp1064Tyr
ENST00000549194.1:n.56G>T
ENST00000550718.1:c.2G>T
NM_024312.4:c.3190G>T	NP_077288.2:p.Asp1064Tyr
XM_006719593.2:c.3190G>T	XP_006719656.1:p.Asp1064Tyr
XM_011538731.1:c.3109G>T	XP_011537033.1:p.Asp1037Tyr
XM_006719593.3:c.3190G>T	XP_006719656.1:p.Asp1064Tyr
XM_011538731.2:c.3109G>T	XP_011537033.1:p.Asp1037Tyr
XM_017019961.1:c.2974G>T	XP_016875450.1:p.Asp992Tyr
XM_017019962.2:c.1963G>T	XP_016875451.1:p.Asp655Tyr
NM_024312.5:c.3190G>T MANE Select	NP_077288.2:p.Asp1064Tyr