Canonical Allele Identifier: CA2058964752
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101785942C= , CM000674.2:g.101785942C= GRCh38
NC_000012.11:g.102179720C= , CM000674.1:g.102179720C= GRCh37
NC_000012.10:g.100703851C= NCBI36
NG_021243.1:g.49926G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.571+70G= MANE Select ENSP00000299314.7:n.571+70G=
ENST00000299314.11:c.571+70G= ENSP00000299314.7:n.571+70G=
ENST00000549940.5:c.571+70G= ENSP00000449150.1:n.571+70G=
ENST00000550352.1:n.435G=
ENST00000552681.1:c.205+70G= ENSP00000449217.1:n.205+70G=
NM_024312.4:c.571+70G= NP_077288.2:n.571+70G=
XM_006719593.2:c.571+70G= XP_006719656.1:n.571+70G=
XM_011538731.1:c.490+70G= XP_011537033.1:n.490+70G=
XM_006719593.3:c.571+70G= XP_006719656.1:n.571+70G=
XM_011538731.2:c.490+70G= XP_011537033.1:n.490+70G=
XM_017019961.1:c.355+70G= XP_016875450.1:n.355+70G=
XM_017019962.2:c.-780+70G= XP_016875451.1:n.-780+70G=
NM_024312.5:c.571+70G= MANE Select NP_077288.2:n.571+70G=