Canonical Allele Identifier: CA799576985
Gene: DSPP HGNC NCBI

Linked Data

dbSNP Id: rs1324367494
gnomAD v4: 4-87612009-A-ATT
MyVariant Identifiers: chr4:g.88533161_88533162insTT (hg19) chr4:g.87612009_87612010insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612011_87612012dup , CM000666.2:g.87612011_87612012dup GRCh38
NC_000004.11:g.88533163_88533164dup , CM000666.1:g.88533163_88533164dup GRCh37
NC_000004.10:g.88752187_88752188dup NCBI36
NG_011595.1:g.8483_8484dup

Transcript Alleles

HGVS Amino-acid change
ENST00000651931.1:c.52-94_52-93dup MANE Select ENSP00000498766.1:n.52-94_52-93dup
ENST00000282478.7:c.52-94_52-93dup ENSP00000282478.7:n.52-94_52-93dup
ENST00000399271.5:c.52-94_52-93dup ENSP00000382213.1:n.52-94_52-93dup
NM_014208.3:c.52-94_52-93dup MANE Select NP_055023.2:n.52-94_52-93dup
Search 100 bp 5'
Search 100 bp 3'