Canonical Allele Identifier: CA386301755

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102161829C>T (hg19) ; chr12:g.101768051C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768051C>T , CM000674.2:g.101768051C>T	GRCh38
NC_000012.11:g.102161829C>T , CM000674.1:g.102161829C>T	GRCh37
NC_000012.10:g.100685960C>T	NCBI36
NG_021243.1:g.67817G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1394G>A MANE Select	ENSP00000299314.7:p.Gly465Asp
ENST00000299314.11:c.1394G>A	ENSP00000299314.7:p.Gly465Asp
ENST00000549940.5:c.1394G>A	ENSP00000449150.1:p.Gly465Asp
ENST00000552009.1:n.53G>A
NM_024312.4:c.1394G>A	NP_077288.2:p.Gly465Asp
XM_006719593.2:c.1394G>A	XP_006719656.1:p.Gly465Asp
XM_011538731.1:c.1313G>A	XP_011537033.1:p.Gly438Asp
XM_006719593.3:c.1394G>A	XP_006719656.1:p.Gly465Asp
XM_011538731.2:c.1313G>A	XP_011537033.1:p.Gly438Asp
XM_017019961.1:c.1178G>A	XP_016875450.1:p.Gly393Asp
XM_017019962.2:c.167G>A	XP_016875451.1:p.Gly56Asp
NM_024312.5:c.1394G>A MANE Select	NP_077288.2:p.Gly465Asp