Canonical Allele Identifier: CA2671358296
Gene: DSPP HGNC NCBI

Linked Data

gnomAD v4: 4-87612010-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612010T>G , CM000666.2:g.87612010T>G GRCh38
NC_000004.11:g.88533162T>G , CM000666.1:g.88533162T>G GRCh37
NC_000004.10:g.88752186T>G NCBI36
NG_011595.1:g.8482T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.52-95T>G MANE Select ENSP00000498766.1:n.52-95T>G
ENST00000282478.7:c.52-95T>G ENSP00000282478.7:n.52-95T>G
ENST00000399271.5:c.52-95T>G ENSP00000382213.1:n.52-95T>G
NM_014208.3:c.52-95T>G MANE Select NP_055023.2:n.52-95T>G
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