Canonical Allele Identifier: CA1474384347
Gene: DSPP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612215A= , CM000666.2:g.87612215A= GRCh38
NC_000004.11:g.88533367A= , CM000666.1:g.88533367A= GRCh37
NC_000004.10:g.88752391A= NCBI36
NG_011595.1:g.8687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.135+27A= MANE Select ENSP00000498766.1:n.135+27A=
ENST00000282478.7:c.135+27A= ENSP00000282478.7:n.135+27A=
ENST00000399271.5:c.135+27A= ENSP00000382213.1:n.135+27A=
NM_014208.3:c.135+27A= MANE Select NP_055023.2:n.135+27A=