Canonical Allele Identifier: CA267586
Gene: GM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 100728
dbSNP Id: rs587779405

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151266820del , CM000667.2:g.151266820del GRCh38
NC_000005.9:g.150646381del , CM000667.1:g.150646381del GRCh37
NC_000005.8:g.150626574del NCBI36
NG_009059.1:g.18769del

Transcript Alleles

HGVS Amino-acid change
ENST00000357164.4:c.333del MANE Select ENSP00000349687.3:p.Cys112ValfsTer7
ENST00000357164.3:c.333del ENSP00000349687.3:p.Cys112ValfsTer7
ENST00000523004.1:c.208del
ENST00000523466.5:c.378del ENSP00000429100.1:p.Cys127ValfsTer7
NM_000405.4:c.333del NP_000396.2:p.Cys112ValfsTer7
NM_001167607.1:c.333del NP_001161079.1:p.Cys112ValfsTer7
NM_000405.5:c.333del MANE Select NP_000396.2:p.Cys112ValfsTer7
NM_001167607.2:c.333del NP_001161079.1:p.Cys112ValfsTer7
NM_001167607.3:c.333del NP_001161079.1:p.Cys112ValfsTer7