Canonical Allele Identifier: CA2762527065
Gene: DSPP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612239T>G , CM000666.2:g.87612239T>G GRCh38
NC_000004.11:g.88533391T>G , CM000666.1:g.88533391T>G GRCh37
NC_000004.10:g.88752415T>G NCBI36
NG_011595.1:g.8711T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.135+51T>G MANE Select ENSP00000498766.1:n.135+51T>G
ENST00000282478.7:c.135+51T>G ENSP00000282478.7:n.135+51T>G
ENST00000399271.5:c.135+51T>G ENSP00000382213.1:n.135+51T>G
NM_014208.3:c.135+51T>G MANE Select NP_055023.2:n.135+51T>G