Canonical Allele Identifier: CA386301726

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102161822A>T (hg19) ; chr12:g.101768044A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768044A>T , CM000674.2:g.101768044A>T	GRCh38
NC_000012.11:g.102161822A>T , CM000674.1:g.102161822A>T	GRCh37
NC_000012.10:g.100685953A>T	NCBI36
NG_021243.1:g.67824T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1401T>A MANE Select	ENSP00000299314.7:p.Asp467Glu
ENST00000299314.11:c.1401T>A	ENSP00000299314.7:p.Asp467Glu
ENST00000549940.5:c.1401T>A	ENSP00000449150.1:p.Asp467Glu
ENST00000552009.1:n.60T>A
NM_024312.4:c.1401T>A	NP_077288.2:p.Asp467Glu
XM_006719593.2:c.1401T>A	XP_006719656.1:p.Asp467Glu
XM_011538731.1:c.1320T>A	XP_011537033.1:p.Asp440Glu
XM_006719593.3:c.1401T>A	XP_006719656.1:p.Asp467Glu
XM_011538731.2:c.1320T>A	XP_011537033.1:p.Asp440Glu
XM_017019961.1:c.1185T>A	XP_016875450.1:p.Asp395Glu
XM_017019962.2:c.174T>A	XP_016875451.1:p.Asp58Glu
NM_024312.5:c.1401T>A MANE Select	NP_077288.2:p.Asp467Glu