Canonical Allele Identifier: CA343342
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 39028
ClinVar RCV Id: RCV000032293
dbSNP Id: rs281864974

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101768162T>C , CM000674.2:g.101768162T>C GRCh38
NC_000012.11:g.102161940T>C , CM000674.1:g.102161940T>C GRCh37
NC_000012.10:g.100686071T>C NCBI36
NG_021243.1:g.67706A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299314.12:c.1285-2A>G MANE Select ENSP00000299314.7:n.1285-2A>G
ENST00000299314.11:c.1285-2A>G ENSP00000299314.7:n.1285-2A>G
ENST00000549940.5:c.1285-2A>G ENSP00000449150.1:n.1285-2A>G
NM_024312.4:c.1285-2A>G NP_077288.2:n.1285-2A>G
XM_006719593.2:c.1285-2A>G XP_006719656.1:n.1285-2A>G
XM_011538731.1:c.1204-2A>G XP_011537033.1:n.1204-2A>G
XM_006719593.3:c.1285-2A>G XP_006719656.1:n.1285-2A>G
XM_011538731.2:c.1204-2A>G XP_011537033.1:n.1204-2A>G
XM_017019961.1:c.1069-2A>G XP_016875450.1:n.1069-2A>G
XM_017019962.2:c.58-2A>G XP_016875451.1:n.58-2A>G
NM_024312.5:c.1285-2A>G MANE Select NP_077288.2:n.1285-2A>G