Canonical Allele Identifier: CA440294100
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533707A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612555A>T , CM000666.2:g.87612555A>T GRCh38
NC_000004.11:g.88533707A>T , CM000666.1:g.88533707A>T GRCh37
NC_000004.10:g.88752731A>T NCBI36
NG_011595.1:g.9027A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.369A>T MANE Select ENSP00000498766.1:p.Gly123=
ENST00000282478.7:c.369A>T ENSP00000282478.7:p.Gly123=
ENST00000399271.5:c.369A>T ENSP00000382213.1:p.Gly123=
NM_014208.3:c.369A>T MANE Select NP_055023.2:p.Gly123=