Canonical Allele Identifier: CA2002735670
Gene: ZPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781414_116781415delinsTA , CM000673.2:g.116781414_116781415delinsTA GRCh38
NC_000011.9:g.116652130_116652131delinsTA , CM000673.1:g.116652130_116652131delinsTA GRCh37
NC_000011.8:g.116157340_116157341delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+743_1179+744delinsTA MANE Select ENSP00000227322.3:n.1179+743_1179+744delinsTA
ENST00000227322.7:c.1179+743_1179+744delinsTA ENSP00000227322.3:n.1179+743_1179+744delinsTA
ENST00000429220.5:c.958+743_958+744delinsTA
ENST00000444935.5:c.1091+1504_1091+1505delinsTA
NM_003904.3:c.1179+743_1179+744delinsTA NP_003895.1:n.1179+743_1179+744delinsTA
NM_001317086.1:c.1017+743_1017+744delinsTA NP_001304015.1:n.1017+743_1017+744delinsTA
NM_003904.4:c.1179+743_1179+744delinsTA NP_003895.1:n.1179+743_1179+744delinsTA
XR_001748023.2:n.2507+743_2507+744delinsTA
NM_003904.5:c.1179+743_1179+744delinsTA MANE Select NP_003895.1:n.1179+743_1179+744delinsTA
NM_001317086.2:c.1017+743_1017+744delinsTA NP_001304015.1:n.1017+743_1017+744delinsTA