Canonical Allele Identifier: CA1474383746
Gene: DSPP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87610898T= , CM000666.2:g.87610898T= GRCh38
NC_000004.11:g.88532050T= , CM000666.1:g.88532050T= GRCh37
NC_000004.10:g.88751074T= NCBI36
NG_011595.1:g.7370T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.-11T= MANE Select ENSP00000498766.1:n.-11T=
ENST00000282478.7:c.-11T= ENSP00000282478.7:n.-11T=
ENST00000399271.5:c.-11T= ENSP00000382213.1:n.-11T=
NM_014208.3:c.-11T= MANE Select NP_055023.2:n.-11T=
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