Canonical Allele Identifier: CA2002735798
Gene: ZPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781694_116781698delinsCAAGA , CM000673.2:g.116781694_116781698delinsCAAGA GRCh38
NC_000011.9:g.116652410_116652414delinsCAAGA , CM000673.1:g.116652410_116652414delinsCAAGA GRCh37
NC_000011.8:g.116157620_116157624delinsCAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+460_1179+464delinsTCTTG MANE Select ENSP00000227322.3:n.1179+460_1179+464delinsTCTTG
ENST00000227322.7:c.1179+460_1179+464delinsTCTTG ENSP00000227322.3:n.1179+460_1179+464delinsTCTTG
ENST00000429220.5:c.958+460_958+464delinsTCTTG
ENST00000444935.5:c.1091+1221_1091+1225delinsTCTTG
NM_003904.3:c.1179+460_1179+464delinsTCTTG NP_003895.1:n.1179+460_1179+464delinsTCTTG
NM_001317086.1:c.1017+460_1017+464delinsTCTTG NP_001304015.1:n.1017+460_1017+464delinsTCTTG
NM_003904.4:c.1179+460_1179+464delinsTCTTG NP_003895.1:n.1179+460_1179+464delinsTCTTG
XR_001748023.2:n.2507+460_2507+464delinsTCTTG
NM_003904.5:c.1179+460_1179+464delinsTCTTG MANE Select NP_003895.1:n.1179+460_1179+464delinsTCTTG
NM_001317086.2:c.1017+460_1017+464delinsTCTTG NP_001304015.1:n.1017+460_1017+464delinsTCTTG