Canonical Allele Identifier: CA2058985309
Gene: GNPTAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830850G= , CM000674.2:g.101830850G= GRCh38
NC_000012.11:g.102224628G= , CM000674.1:g.102224628G= GRCh37
NC_000012.10:g.100748759G= NCBI36
NG_021243.1:g.5018C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-175C= MANE Select ENSP00000299314.7:n.-175C=
ENST00000299314.11:c.-175C= ENSP00000299314.7:n.-175C=
NM_024312.4:c.-175C= NP_077288.2:n.-175C=
XM_006719593.2:c.-175C= XP_006719656.1:n.-175C=
NM_024312.5:c.-175C= MANE Select NP_077288.2:n.-175C=