Canonical Allele Identifier: CA601828476
Gene: ZPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1225969554
gnomAD v2: 11-116648979-CCTCTGTT-C
gnomAD v3: 11-116778263-CCTCTGTT-C
gnomAD v4: 11-116778263-CCTCTGTT-C
MyVariant Identifiers: chr11:g.116648980_116648986del (hg19) chr11:g.116778264_116778270del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116778266_116778272del , CM000673.2:g.116778266_116778272del GRCh38
NC_000011.9:g.116648982_116648988del , CM000673.1:g.116648982_116648988del GRCh37
NC_000011.8:g.116154192_116154198del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.*655_*661del MANE Select ENSP00000227322.3:n.*655_*661del
ENST00000227322.7:c.*655_*661del ENSP00000227322.3:n.*655_*661del
ENST00000429220.5:c.1814_1820del
ENST00000444935.5:c.1947_1953del
NM_001317086.1:c.*655_*661del NP_001304015.1:n.*655_*661del
NM_003904.4:c.*655_*661del NP_003895.1:n.*655_*661del
NM_003904.5:c.*655_*661del MANE Select NP_003895.1:n.*655_*661del
NM_001317086.2:c.*655_*661del NP_001304015.1:n.*655_*661del
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