Canonical Allele Identifier: CA672170265
Gene: ZPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1319073979
MyVariant Identifiers: chr11:g.116652131del (hg19) chr11:g.116781415del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781418del , CM000673.2:g.116781418del GRCh38
NC_000011.9:g.116652134del , CM000673.1:g.116652134del GRCh37
NC_000011.8:g.116157344del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+743del MANE Select ENSP00000227322.3:n.1179+743del
ENST00000227322.7:c.1179+743del ENSP00000227322.3:n.1179+743del
ENST00000429220.5:c.958+743del
ENST00000444935.5:c.1091+1504del
NM_003904.3:c.1179+743del NP_003895.1:n.1179+743del
NM_001317086.1:c.1017+743del NP_001304015.1:n.1017+743del
NM_003904.4:c.1179+743del NP_003895.1:n.1179+743del
XR_001748023.2:n.2507+743del
NM_003904.5:c.1179+743del MANE Select NP_003895.1:n.1179+743del
NM_001317086.2:c.1017+743del NP_001304015.1:n.1017+743del
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