Canonical Allele Identifier: CA2695221404
Community Standard Title: NC_000016.10:g.1362535del
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362535del , CM000678.2:g.1362535del GRCh38
NC_000016.9:g.1412536del , CM000678.1:g.1412536del GRCh37
NC_000016.8:g.1352537del NCBI36
NG_016985.1:g.15637del
NG_033129.1:g.57171del

Transcript Alleles

HGVS Amino-acid Change
NM_032520.4:c.609+1del
NM_032520.5:c.609+1del
ENST00000204679.8:c.609+1del
ENST00000204679.9:c.609+1del
ENST00000527076.1:n.1757del
ENST00000527168.5:n.776+1del
ENST00000527168.6:n.708+1del
ENST00000529110.2:c.693+1del
ENST00000529957.5:n.708+1del
ENST00000529957.6:n.667+1del
ENST00000683366.1:c.*341+1del
ENST00000683887.1:c.657+1del
ENST00000684100.1:n.603+1del
ENST00000684126.1:n.668del
ENST00000684688.1:n.1234+1del
XM_017023782.1:c.657+1del
XM_017023783.1:c.249+1del