Canonical Allele Identifier: CA357603454
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1727757259

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612572A>G , CM000666.2:g.87612572A>G GRCh38
NC_000004.11:g.88533724A>G , CM000666.1:g.88533724A>G GRCh37
NC_000004.10:g.88752748A>G NCBI36
NG_011595.1:g.9044A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.386A>G MANE Select ENSP00000498766.1:p.Glu129Gly
ENST00000282478.7:c.386A>G ENSP00000282478.7:p.Glu129Gly
ENST00000399271.5:c.386A>G ENSP00000382213.1:p.Glu129Gly
NM_014208.3:c.386A>G MANE Select NP_055023.2:p.Glu129Gly