Canonical Allele Identifier: CA357603056
Gene: DSPP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612396G>C , CM000666.2:g.87612396G>C GRCh38
NC_000004.11:g.88533548G>C , CM000666.1:g.88533548G>C GRCh37
NC_000004.10:g.88752572G>C NCBI36
NG_011595.1:g.8868G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.210G>C MANE Select ENSP00000498766.1:p.Glu70Asp
ENST00000282478.7:c.210G>C ENSP00000282478.7:p.Glu70Asp
ENST00000399271.5:c.210G>C ENSP00000382213.1:p.Glu70Asp
NM_014208.3:c.210G>C MANE Select NP_055023.2:p.Glu70Asp