Canonical Allele Identifier: CA100849721
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs35337797
MyVariant Identifiers: chr4:g.88533830_88533831insG (hg19) chr4:g.87612678_87612679insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612682dup , CM000666.2:g.87612682dup GRCh38
NC_000004.11:g.88533834dup , CM000666.1:g.88533834dup GRCh37
NC_000004.10:g.88752858dup NCBI36
NG_011595.1:g.9154dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.496dup MANE Select ENSP00000498766.1:p.Asp166GlyfsTer9
ENST00000282478.7:c.496dup ENSP00000282478.7:p.Asp166GlyfsTer9
ENST00000399271.5:c.496dup ENSP00000382213.1:p.Asp166GlyfsTer9
NM_014208.3:c.496dup MANE Select NP_055023.2:p.Asp166GlyfsTer9
Search 100 bp 5'
Search 100 bp 3'