Canonical Allele Identifier: CA440294062
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533512T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612360T>A , CM000666.2:g.87612360T>A GRCh38
NC_000004.11:g.88533512T>A , CM000666.1:g.88533512T>A GRCh37
NC_000004.10:g.88752536T>A NCBI36
NG_011595.1:g.8832T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.174T>A MANE Select ENSP00000498766.1:p.Gly58=
ENST00000282478.7:c.174T>A ENSP00000282478.7:p.Gly58=
ENST00000399271.5:c.174T>A ENSP00000382213.1:p.Gly58=
NM_014208.3:c.174T>A MANE Select NP_055023.2:p.Gly58=
Search 100 bp 5'
Search 100 bp 3'