Canonical Allele Identifier: CA357603034
Gene: DSPP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88533538G>T (hg19) chr4:g.87612386G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612386G>T , CM000666.2:g.87612386G>T GRCh38
NC_000004.11:g.88533538G>T , CM000666.1:g.88533538G>T GRCh37
NC_000004.10:g.88752562G>T NCBI36
NG_011595.1:g.8858G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.200G>T MANE Select ENSP00000498766.1:p.Gly67Val
ENST00000282478.7:c.200G>T ENSP00000282478.7:p.Gly67Val
ENST00000399271.5:c.200G>T ENSP00000382213.1:p.Gly67Val
NM_014208.3:c.200G>T MANE Select NP_055023.2:p.Gly67Val
Search 100 bp 5'
Search 100 bp 3'