Canonical Allele Identifier: CA386296187

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155393G>C (hg19) ; chr12:g.101761615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761615G>C , CM000674.2:g.101761615G>C	GRCh38
NC_000012.11:g.102155393G>C , CM000674.1:g.102155393G>C	GRCh37
NC_000012.10:g.100679524G>C	NCBI36
NG_021243.1:g.74253C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2864C>G MANE Select	ENSP00000299314.7:p.Ala955Gly
ENST00000299314.11:c.2864C>G	ENSP00000299314.7:p.Ala955Gly
NM_024312.4:c.2864C>G	NP_077288.2:p.Ala955Gly
XM_006719593.2:c.2864C>G	XP_006719656.1:p.Ala955Gly
XM_011538731.1:c.2783C>G	XP_011537033.1:p.Ala928Gly
XM_006719593.3:c.2864C>G	XP_006719656.1:p.Ala955Gly
XM_011538731.2:c.2783C>G	XP_011537033.1:p.Ala928Gly
XM_017019961.1:c.2648C>G	XP_016875450.1:p.Ala883Gly
XM_017019962.2:c.1637C>G	XP_016875451.1:p.Ala546Gly
NM_024312.5:c.2864C>G MANE Select	NP_077288.2:p.Ala955Gly