Canonical Allele Identifier: CA2002735652
Gene: ZPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781373A= , CM000673.2:g.116781373A= GRCh38
NC_000011.9:g.116652089A= , CM000673.1:g.116652089A= GRCh37
NC_000011.8:g.116157299A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+785T= MANE Select ENSP00000227322.3:n.1179+785T=
ENST00000227322.7:c.1179+785T= ENSP00000227322.3:n.1179+785T=
ENST00000429220.5:c.958+785T=
ENST00000444935.5:c.1092-1536T=
NM_003904.3:c.1179+785T= NP_003895.1:n.1179+785T=
NM_001317086.1:c.1017+785T= NP_001304015.1:n.1017+785T=
NM_003904.4:c.1179+785T= NP_003895.1:n.1179+785T=
XR_001748023.2:n.2507+785T=
NM_003904.5:c.1179+785T= MANE Select NP_003895.1:n.1179+785T=
NM_001317086.2:c.1017+785T= NP_001304015.1:n.1017+785T=