Canonical Allele Identifier: CA2058985304
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830844G= , CM000674.2:g.101830844G= GRCh38
NC_000012.11:g.102224622G= , CM000674.1:g.102224622G= GRCh37
NC_000012.10:g.100748753G= NCBI36
NG_021243.1:g.5024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-169C= MANE Select ENSP00000299314.7:n.-169C=
ENST00000299314.11:c.-169C= ENSP00000299314.7:n.-169C=
NM_024312.4:c.-169C= NP_077288.2:n.-169C=
XM_006719593.2:c.-169C= XP_006719656.1:n.-169C=
NM_024312.5:c.-169C= MANE Select NP_077288.2:n.-169C=