Canonical Allele Identifier: CA2002735796
Gene: ZPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781688_116781691delinsGAAA , CM000673.2:g.116781688_116781691delinsGAAA GRCh38
NC_000011.9:g.116652404_116652407delinsGAAA , CM000673.1:g.116652404_116652407delinsGAAA GRCh37
NC_000011.8:g.116157614_116157617delinsGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+467_1179+470delinsTTTC MANE Select ENSP00000227322.3:n.1179+467_1179+470delinsTTTC
ENST00000227322.7:c.1179+467_1179+470delinsTTTC ENSP00000227322.3:n.1179+467_1179+470delinsTTTC
ENST00000429220.5:c.958+467_958+470delinsTTTC
ENST00000444935.5:c.1091+1228_1091+1231delinsTTTC
NM_003904.3:c.1179+467_1179+470delinsTTTC NP_003895.1:n.1179+467_1179+470delinsTTTC
NM_001317086.1:c.1017+467_1017+470delinsTTTC NP_001304015.1:n.1017+467_1017+470delinsTTTC
NM_003904.4:c.1179+467_1179+470delinsTTTC NP_003895.1:n.1179+467_1179+470delinsTTTC
XR_001748023.2:n.2507+467_2507+470delinsTTTC
NM_003904.5:c.1179+467_1179+470delinsTTTC MANE Select NP_003895.1:n.1179+467_1179+470delinsTTTC
NM_001317086.2:c.1017+467_1017+470delinsTTTC NP_001304015.1:n.1017+467_1017+470delinsTTTC