Canonical Allele Identifier: CA1474383729
Gene: DSPP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87610867C= , CM000666.2:g.87610867C= GRCh38
NC_000004.11:g.88532019C= , CM000666.1:g.88532019C= GRCh37
NC_000004.10:g.88751043C= NCBI36
NG_011595.1:g.7339C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.-28-14C= MANE Select ENSP00000498766.1:n.-28-14C=
ENST00000399271.5:c.-28-14C= ENSP00000382213.1:n.-28-14C=
NM_014208.3:c.-28-14C= MANE Select NP_055023.2:n.-28-14C=