Canonical Allele Identifier: CA357603059

Gene: DSPP

Linked Data

• gnomAD v4: 4-87612397-A-G
• MyVariant Identifiers: chr4:g.88533549A>G (hg19) ; chr4:g.87612397A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87612397A>G , CM000666.2:g.87612397A>G	GRCh38
NC_000004.11:g.88533549A>G , CM000666.1:g.88533549A>G	GRCh37
NC_000004.10:g.88752573A>G	NCBI36
NG_011595.1:g.8869A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651931.1:c.211A>G MANE Select	ENSP00000498766.1:p.Asn71Asp
ENST00000282478.7:c.211A>G	ENSP00000282478.7:p.Asn71Asp
ENST00000399271.5:c.211A>G	ENSP00000382213.1:p.Asn71Asp
NM_014208.3:c.211A>G MANE Select	NP_055023.2:p.Asn71Asp