Canonical Allele Identifier: CA2671358389
Gene: DSPP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612458del , CM000666.2:g.87612458del GRCh38
NC_000004.11:g.88533610del , CM000666.1:g.88533610del GRCh37
NC_000004.10:g.88752634del NCBI36
NG_011595.1:g.8930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.272del MANE Select ENSP00000498766.1:p.Lys91ArgfsTer9
ENST00000282478.7:c.272del ENSP00000282478.7:p.Lys91ArgfsTer9
ENST00000399271.5:c.272del ENSP00000382213.1:p.Lys91ArgfsTer9
NM_014208.3:c.272del MANE Select NP_055023.2:p.Lys91ArgfsTer9