Canonical Allele Identifier: CA2671358355
Gene: DSPP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612195del , CM000666.2:g.87612195del GRCh38
NC_000004.11:g.88533347del , CM000666.1:g.88533347del GRCh37
NC_000004.10:g.88752371del NCBI36
NG_011595.1:g.8667del

Transcript Alleles

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