Canonical Allele Identifier: CA357603721
Gene: DSPP HGNC NCBI

Linked Data

gnomAD v4: 4-87612692-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612692A>G , CM000666.2:g.87612692A>G GRCh38
NC_000004.11:g.88533844A>G , CM000666.1:g.88533844A>G GRCh37
NC_000004.10:g.88752868A>G NCBI36
NG_011595.1:g.9164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.506A>G MANE Select ENSP00000498766.1:p.Asp169Gly
ENST00000282478.7:c.506A>G ENSP00000282478.7:p.Asp169Gly
ENST00000399271.5:c.506A>G ENSP00000382213.1:p.Asp169Gly
NM_014208.3:c.506A>G MANE Select NP_055023.2:p.Asp169Gly