Canonical Allele Identifier: CA1474384563
Gene: DSPP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.506A= MANE Select ENSP00000498766.1:p.Asp169=
ENST00000282478.7:c.506A= ENSP00000282478.7:p.Asp169=
ENST00000399271.5:c.506A= ENSP00000382213.1:p.Asp169=
NM_014208.3:c.506A= MANE Select NP_055023.2:p.Asp169=