Canonical Allele Identifier: CA2058950567
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101753449C= , CM000674.2:g.101753449C= GRCh38
NC_000012.11:g.102147227C= , CM000674.1:g.102147227C= GRCh37
NC_000012.10:g.100671358C= NCBI36
NG_021243.1:g.82419G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.3525G= MANE Select ENSP00000299314.7:p.Met1175=
ENST00000299314.11:c.3525G= ENSP00000299314.7:p.Met1175=
ENST00000549738.5:c.423G= ENSP00000450161.1:n.423G=
NM_024312.4:c.3525G= NP_077288.2:p.Met1175=
XM_011538731.1:c.3444G= XP_011537033.1:p.Met1148=
XM_011538731.2:c.3444G= XP_011537033.1:p.Met1148=
XM_017019961.1:c.3309G= XP_016875450.1:p.Met1103=
XM_017019962.2:c.2298G= XP_016875451.1:p.Met766=
NM_024312.5:c.3525G= MANE Select NP_077288.2:p.Met1175=