Canonical Allele Identifier: CA2671358362
Gene: DSPP HGNC NCBI

Linked Data

gnomAD v4: 4-87612213-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612213T>A , CM000666.2:g.87612213T>A GRCh38
NC_000004.11:g.88533365T>A , CM000666.1:g.88533365T>A GRCh37
NC_000004.10:g.88752389T>A NCBI36
NG_011595.1:g.8685T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.135+25T>A MANE Select ENSP00000498766.1:n.135+25T>A
ENST00000282478.7:c.135+25T>A ENSP00000282478.7:n.135+25T>A
ENST00000399271.5:c.135+25T>A ENSP00000382213.1:n.135+25T>A
NM_014208.3:c.135+25T>A MANE Select NP_055023.2:n.135+25T>A