Canonical Allele Identifier: CA2601492296
Gene: DSPP HGNC NCBI

Linked Data

gnomAD v3: 4-87612224-T-G
gnomAD v4: 4-87612224-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612224T>G , CM000666.2:g.87612224T>G GRCh38
NC_000004.11:g.88533376T>G , CM000666.1:g.88533376T>G GRCh37
NC_000004.10:g.88752400T>G NCBI36
NG_011595.1:g.8696T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.135+36T>G MANE Select ENSP00000498766.1:n.135+36T>G
ENST00000282478.7:c.135+36T>G ENSP00000282478.7:n.135+36T>G
ENST00000399271.5:c.135+36T>G ENSP00000382213.1:n.135+36T>G
NM_014208.3:c.135+36T>G MANE Select NP_055023.2:n.135+36T>G