Canonical Allele Identifier: CA590937556
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1280326584
gnomAD v2: 9-128003964-AG-A
gnomAD v3: 9-125241685-AG-A
gnomAD v4: 9-125241685-AG-A
MyVariant Identifiers: chr9:g.128003965del (hg19) chr9:g.125241686del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241690del , CM000671.2:g.125241690del GRCh38
NC_000009.11:g.128003969del , CM000671.1:g.128003969del GRCh37
NC_000009.10:g.127043790del NCBI36
NG_027761.1:g.4702del

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-715del (GAPVD1) XP_011516803.1:n.-715del
XM_011518503.1:c.-1021del (GAPVD1) XP_011516805.1:n.-1021del
XM_011518504.1:c.-666del (GAPVD1) XP_011516806.1:n.-666del
XR_001746927.1:n.28del (HSPA5-DT)
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