Canonical Allele Identifier: CA2058964726
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101785867A= , CM000674.2:g.101785867A= GRCh38
NC_000012.11:g.102179645A= , CM000674.1:g.102179645A= GRCh37
NC_000012.10:g.100703776A= NCBI36
NG_021243.1:g.50001T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.571+145T= MANE Select ENSP00000299314.7:n.571+145T=
ENST00000299314.11:c.571+145T= ENSP00000299314.7:n.571+145T=
ENST00000549940.5:c.571+145T= ENSP00000449150.1:n.571+145T=
ENST00000550352.1:n.510T=
ENST00000552681.1:c.205+145T= ENSP00000449217.1:n.205+145T=
NM_024312.4:c.571+145T= NP_077288.2:n.571+145T=
XM_006719593.2:c.571+145T= XP_006719656.1:n.571+145T=
XM_011538731.1:c.490+145T= XP_011537033.1:n.490+145T=
XM_006719593.3:c.571+145T= XP_006719656.1:n.571+145T=
XM_011538731.2:c.490+145T= XP_011537033.1:n.490+145T=
XM_017019961.1:c.355+145T= XP_016875450.1:n.355+145T=
XM_017019962.2:c.-780+145T= XP_016875451.1:n.-780+145T=
NM_024312.5:c.571+145T= MANE Select NP_077288.2:n.571+145T=