Canonical Allele Identifier: CA100849477
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs905226892
gnomAD v4: 4-87612425-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612425G>A , CM000666.2:g.87612425G>A GRCh38
NC_000004.11:g.88533577G>A , CM000666.1:g.88533577G>A GRCh37
NC_000004.10:g.88752601G>A NCBI36
NG_011595.1:g.8897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.239G>A MANE Select ENSP00000498766.1:p.Gly80Glu
ENST00000282478.7:c.239G>A ENSP00000282478.7:p.Gly80Glu
ENST00000399271.5:c.239G>A ENSP00000382213.1:p.Gly80Glu
NM_014208.3:c.239G>A MANE Select NP_055023.2:p.Gly80Glu