Canonical Allele Identifier: CA553085318
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1349072672
gnomAD v2: 4-88533442-A-G
gnomAD v4: 4-87612290-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612290A>G , CM000666.2:g.87612290A>G GRCh38
NC_000004.11:g.88533442A>G , CM000666.1:g.88533442A>G GRCh37
NC_000004.10:g.88752466A>G NCBI36
NG_011595.1:g.8762A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.136-32A>G MANE Select ENSP00000498766.1:n.136-32A>G
ENST00000282478.7:c.136-32A>G ENSP00000282478.7:n.136-32A>G
ENST00000399271.5:c.136-32A>G ENSP00000382213.1:n.136-32A>G
NM_014208.3:c.136-32A>G MANE Select NP_055023.2:n.136-32A>G