Canonical Allele Identifier: CA1474384541
Gene: DSPP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612649A= , CM000666.2:g.87612649A= GRCh38
NC_000004.11:g.88533801A= , CM000666.1:g.88533801A= GRCh37
NC_000004.10:g.88752825A= NCBI36
NG_011595.1:g.9121A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.463A= MANE Select ENSP00000498766.1:p.Asn155=
ENST00000282478.7:c.463A= ENSP00000282478.7:p.Asn155=
ENST00000399271.5:c.463A= ENSP00000382213.1:p.Asn155=
NM_014208.3:c.463A= MANE Select NP_055023.2:p.Asn155=
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