Canonical Allele Identifier: CA100849066
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs36228864
gnomAD v2: 4-88533163-TTGTGTGTGTG-T
gnomAD v3: 4-87612011-TTGTGTGTGTG-T
gnomAD v4: 4-87612011-TTGTGTGTGTG-T
MyVariant Identifiers: chr4:g.88533164_88533173del (hg19) chr4:g.87612012_87612021del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612032_87612041del , CM000666.2:g.87612032_87612041del GRCh38
NC_000004.11:g.88533184_88533193del , CM000666.1:g.88533184_88533193del GRCh37
NC_000004.10:g.88752208_88752217del NCBI36
NG_011595.1:g.8504_8513del

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.52-73_52-64del MANE Select ENSP00000498766.1:n.52-73_52-64del
ENST00000282478.7:c.52-73_52-64del ENSP00000282478.7:n.52-73_52-64del
ENST00000399271.5:c.52-73_52-64del ENSP00000382213.1:n.52-73_52-64del
NM_014208.3:c.52-73_52-64del MANE Select NP_055023.2:n.52-73_52-64del
Search 100 bp 5'
Search 100 bp 3'