Canonical Allele Identifier: CA2058964761
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101785976T= , CM000674.2:g.101785976T= GRCh38
NC_000012.11:g.102179754T= , CM000674.1:g.102179754T= GRCh37
NC_000012.10:g.100703885T= NCBI36
NG_021243.1:g.49892A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.571+36A= MANE Select ENSP00000299314.7:n.571+36A=
ENST00000299314.11:c.571+36A= ENSP00000299314.7:n.571+36A=
ENST00000549940.5:c.571+36A= ENSP00000449150.1:n.571+36A=
ENST00000550352.1:n.401A=
ENST00000552681.1:c.205+36A= ENSP00000449217.1:n.205+36A=
NM_024312.4:c.571+36A= NP_077288.2:n.571+36A=
XM_006719593.2:c.571+36A= XP_006719656.1:n.571+36A=
XM_011538731.1:c.490+36A= XP_011537033.1:n.490+36A=
XM_006719593.3:c.571+36A= XP_006719656.1:n.571+36A=
XM_011538731.2:c.490+36A= XP_011537033.1:n.490+36A=
XM_017019961.1:c.355+36A= XP_016875450.1:n.355+36A=
XM_017019962.2:c.-780+36A= XP_016875451.1:n.-780+36A=
NM_024312.5:c.571+36A= MANE Select NP_077288.2:n.571+36A=