Canonical Allele Identifier: CA440294142
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533560T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612408T>C , CM000666.2:g.87612408T>C GRCh38
NC_000004.11:g.88533560T>C , CM000666.1:g.88533560T>C GRCh37
NC_000004.10:g.88752584T>C NCBI36
NG_011595.1:g.8880T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.222T>C MANE Select ENSP00000498766.1:p.Asp74=
ENST00000282478.7:c.222T>C ENSP00000282478.7:p.Asp74=
ENST00000399271.5:c.222T>C ENSP00000382213.1:p.Asp74=
NM_014208.3:c.222T>C MANE Select NP_055023.2:p.Asp74=
Search 100 bp 5'
Search 100 bp 3'