Canonical Allele Identifier: CA553085322
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1226254428
gnomAD v2: 4-88533458-A-G
gnomAD v4: 4-87612306-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612306A>G , CM000666.2:g.87612306A>G GRCh38
NC_000004.11:g.88533458A>G , CM000666.1:g.88533458A>G GRCh37
NC_000004.10:g.88752482A>G NCBI36
NG_011595.1:g.8778A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.136-16A>G MANE Select ENSP00000498766.1:n.136-16A>G
ENST00000282478.7:c.136-16A>G ENSP00000282478.7:n.136-16A>G
ENST00000399271.5:c.136-16A>G ENSP00000382213.1:n.136-16A>G
NM_014208.3:c.136-16A>G MANE Select NP_055023.2:n.136-16A>G