Canonical Allele Identifier: CA2002735655
Gene: ZPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1940802613

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116781376T>G , CM000673.2:g.116781376T>G GRCh38
NC_000011.9:g.116652092T>G , CM000673.1:g.116652092T>G GRCh37
NC_000011.8:g.116157302T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227322.8:c.1179+782A>C MANE Select ENSP00000227322.3:n.1179+782A>C
ENST00000227322.7:c.1179+782A>C ENSP00000227322.3:n.1179+782A>C
ENST00000429220.5:c.958+782A>C
ENST00000444935.5:c.1092-1539A>C
NM_003904.3:c.1179+782A>C NP_003895.1:n.1179+782A>C
NM_001317086.1:c.1017+782A>C NP_001304015.1:n.1017+782A>C
NM_003904.4:c.1179+782A>C NP_003895.1:n.1179+782A>C
XR_001748023.2:n.2507+782A>C
NM_003904.5:c.1179+782A>C MANE Select NP_003895.1:n.1179+782A>C
NM_001317086.2:c.1017+782A>C NP_001304015.1:n.1017+782A>C