Canonical Allele Identifier: CA1474384318
Gene: DSPP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612128G= , CM000666.2:g.87612128G= GRCh38
NC_000004.11:g.88533280G= , CM000666.1:g.88533280G= GRCh37
NC_000004.10:g.88752304G= NCBI36
NG_011595.1:g.8600G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.75G= MANE Select ENSP00000498766.1:p.Glu25=
ENST00000282478.7:c.75G= ENSP00000282478.7:p.Glu25=
ENST00000399271.5:c.75G= ENSP00000382213.1:p.Glu25=
NM_014208.3:c.75G= MANE Select NP_055023.2:p.Glu25=