Canonical Allele Identifier: CA2058964794
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101786046A= , CM000674.2:g.101786046A= GRCh38
NC_000012.11:g.102179824A= , CM000674.1:g.102179824A= GRCh37
NC_000012.10:g.100703955A= NCBI36
NG_021243.1:g.49822T=

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.537T= MANE Select ENSP00000299314.7:p.Asn179=
ENST00000299314.11:c.537T= ENSP00000299314.7:p.Asn179=
ENST00000549940.5:c.537T= ENSP00000449150.1:p.Asn179=
ENST00000550352.1:n.331T=
ENST00000552681.1:c.171T= ENSP00000449217.1:p.Asn57=
NM_024312.4:c.537T= NP_077288.2:p.Asn179=
XM_006719593.2:c.537T= XP_006719656.1:p.Asn179=
XM_011538731.1:c.456T= XP_011537033.1:p.Asn152=
XM_006719593.3:c.537T= XP_006719656.1:p.Asn179=
XM_011538731.2:c.456T= XP_011537033.1:p.Asn152=
XM_017019961.1:c.321T= XP_016875450.1:p.Asn107=
XM_017019962.2:c.-814T= XP_016875451.1:n.-814T=
NM_024312.5:c.537T= MANE Select NP_077288.2:p.Asn179=