Canonical Allele Identifier: CA386296298
Gene: GNPTAB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101761664T>G , CM000674.2:g.101761664T>G GRCh38
NC_000012.11:g.102155442T>G , CM000674.1:g.102155442T>G GRCh37
NC_000012.10:g.100679573T>G NCBI36
NG_021243.1:g.74204A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.2815A>C MANE Select ENSP00000299314.7:p.Asn939His
ENST00000299314.11:c.2815A>C ENSP00000299314.7:p.Asn939His
NM_024312.4:c.2815A>C NP_077288.2:p.Asn939His
XM_006719593.2:c.2815A>C XP_006719656.1:p.Asn939His
XM_011538731.1:c.2734A>C XP_011537033.1:p.Asn912His
XM_006719593.3:c.2815A>C XP_006719656.1:p.Asn939His
XM_011538731.2:c.2734A>C XP_011537033.1:p.Asn912His
XM_017019961.1:c.2599A>C XP_016875450.1:p.Asn867His
XM_017019962.2:c.1588A>C XP_016875451.1:p.Asn530His
NM_024312.5:c.2815A>C MANE Select NP_077288.2:p.Asn939His