Canonical Allele Identifier: CA799577312
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1231303747
gnomAD v3: 4-87612236-A-T
gnomAD v4: 4-87612236-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612236A>T , CM000666.2:g.87612236A>T GRCh38
NC_000004.11:g.88533388A>T , CM000666.1:g.88533388A>T GRCh37
NC_000004.10:g.88752412A>T NCBI36
NG_011595.1:g.8708A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.135+48A>T MANE Select ENSP00000498766.1:n.135+48A>T
ENST00000282478.7:c.135+48A>T ENSP00000282478.7:n.135+48A>T
ENST00000399271.5:c.135+48A>T ENSP00000382213.1:n.135+48A>T
NM_014208.3:c.135+48A>T MANE Select NP_055023.2:n.135+48A>T