Canonical Allele Identifier: CA386292266
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753415C>A , CM000674.2:g.101753415C>A GRCh38
NC_000012.11:g.102147193C>A , CM000674.1:g.102147193C>A GRCh37
NC_000012.10:g.100671324C>A NCBI36
NG_021243.1:g.82453G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.3559G>T MANE Select ENSP00000299314.7:p.Glu1187Ter
ENST00000299314.11:c.3559G>T ENSP00000299314.7:p.Glu1187Ter
ENST00000549738.5:c.457G>T ENSP00000450161.1:n.457G>T
NM_024312.4:c.3559G>T NP_077288.2:p.Glu1187Ter
XM_011538731.1:c.3478G>T XP_011537033.1:p.Glu1160Ter
XM_011538731.2:c.3478G>T XP_011537033.1:p.Glu1160Ter
XM_017019961.1:c.3343G>T XP_016875450.1:p.Glu1115Ter
XM_017019962.2:c.2332G>T XP_016875451.1:p.Glu778Ter
NM_024312.5:c.3559G>T MANE Select NP_077288.2:p.Glu1187Ter