Canonical Allele Identifier: CA386292506

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102147243T>C (hg19) ; chr12:g.101753465T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101753465T>C , CM000674.2:g.101753465T>C	GRCh38
NC_000012.11:g.102147243T>C , CM000674.1:g.102147243T>C	GRCh37
NC_000012.10:g.100671374T>C	NCBI36
NG_021243.1:g.82403A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3509A>G MANE Select	ENSP00000299314.7:p.Asp1170Gly
ENST00000299314.11:c.3509A>G	ENSP00000299314.7:p.Asp1170Gly
ENST00000549738.5:c.407A>G	ENSP00000450161.1:n.407A>G
NM_024312.4:c.3509A>G	NP_077288.2:p.Asp1170Gly
XM_011538731.1:c.3428A>G	XP_011537033.1:p.Asp1143Gly
XM_011538731.2:c.3428A>G	XP_011537033.1:p.Asp1143Gly
XM_017019961.1:c.3293A>G	XP_016875450.1:p.Asp1098Gly
XM_017019962.2:c.2282A>G	XP_016875451.1:p.Asp761Gly
NM_024312.5:c.3509A>G MANE Select	NP_077288.2:p.Asp1170Gly