Canonical Allele Identifier: CA229326267
Gene: ZPR1 HGNC NCBI

Linked Data

dbSNP Id: rs995201416
gnomAD v3: 11-116778535-T-C
gnomAD v4: 11-116778535-T-C
MyVariant Identifiers: chr11:g.116649251T>C (hg19) chr11:g.116778535T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116778535T>C , CM000673.2:g.116778535T>C GRCh38
NC_000011.9:g.116649251T>C , CM000673.1:g.116649251T>C GRCh37
NC_000011.8:g.116154461T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.*390A>G MANE Select ENSP00000227322.3:n.*390A>G
ENST00000227322.7:c.*390A>G ENSP00000227322.3:n.*390A>G
ENST00000429220.5:c.1549A>G
ENST00000444935.5:c.1682A>G
NM_001317086.1:c.*390A>G NP_001304015.1:n.*390A>G
NM_003904.4:c.*390A>G NP_003895.1:n.*390A>G
NM_003904.5:c.*390A>G MANE Select NP_003895.1:n.*390A>G
NM_001317086.2:c.*390A>G NP_001304015.1:n.*390A>G
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