Canonical Allele Identifier: CA2058985380
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830916G= , CM000674.2:g.101830916G= GRCh38
NC_000012.11:g.102224694G= , CM000674.1:g.102224694G= GRCh37
NC_000012.10:g.100748825G= NCBI36
NG_021243.1:g.4952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-241C= MANE Select ENSP00000299314.7:n.-241C=
ENST00000299314.11:c.-241C= ENSP00000299314.7:n.-241C=
NM_024312.5:c.-241C= MANE Select NP_077288.2:n.-241C=