Canonical Allele Identifier: CA440293878
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533262T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612110T>A , CM000666.2:g.87612110T>A GRCh38
NC_000004.11:g.88533262T>A , CM000666.1:g.88533262T>A GRCh37
NC_000004.10:g.88752286T>A NCBI36
NG_011595.1:g.8582T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.57T>A MANE Select ENSP00000498766.1:p.Pro19=
ENST00000282478.7:c.57T>A ENSP00000282478.7:p.Pro19=
ENST00000399271.5:c.57T>A ENSP00000382213.1:p.Pro19=
NM_014208.3:c.57T>A MANE Select NP_055023.2:p.Pro19=
Search 100 bp 5'
Search 100 bp 3'