Canonical Allele Identifier: CA15728557
Gene: ZNF664 HGNC NCBI
RFLNA HGNC NCBI

Linked Data

dbSNP Id: rs4765127

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123975620G>T , CM000674.2:g.123975620G>T GRCh38
NC_000012.11:g.124460167G>T , CM000674.1:g.124460167G>T GRCh37
NC_000012.10:g.123026120G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337815.9:c.-757+1600G>T (ZNF664) MANE Select ENSP00000337320.4:n.-757+1600G>T
ENST00000337815.8:c.-757+1600G>T (ZNF664) ENSP00000337320.4:n.-757+1600G>T
ENST00000389727.8:c.-234+1600G>T (RFLNA) ENSP00000374377.4:n.-234+1600G>T
ENST00000392404.7:c.-754+1600G>T (ZNF664) ENSP00000376205.3:n.-754+1600G>T
ENST00000537532.5:n.172+1600G>T (ZNF664)
ENST00000538932.6:c.-754+1600G>T (ZNF664) ENSP00000440645.1:n.-754+1600G>T
ENST00000539257.5:n.164+1600G>T (ZNF664)
ENST00000539644.5:c.-933+1600G>T (ZNF664) ENSP00000441405.1:n.-933+1600G>T
ENST00000541448.5:n.273+1600G>T (ZNF664)
ENST00000542493.5:n.198+1600G>T (ZNF664)
ENST00000543017.5:n.166+1600G>T (ZNF664)
ENST00000545615.1:n.194+1600G>T (RFLNA)
ENST00000546098.5:n.162+1600G>T (ZNF664)
ENST00000618862.1:c.77+1600G>T
NM_001204298.1:c.-754+1600G>T (ZNF664) NP_001191227.1:n.-754+1600G>T
NM_001204299.1:c.-234+1600G>T NP_001191228.1:n.-234+1600G>T
NM_152437.2:c.-757+1600G>T (ZNF664) NP_689650.1:n.-757+1600G>T
NM_001204299.2:c.-234+1600G>T NP_001191228.1:n.-234+1600G>T
NM_001347902.1:c.-234+1600G>T NP_001334831.1:n.-234+1600G>T
NM_152437.3:c.-757+1600G>T (ZNF664) MANE Select NP_689650.1:n.-757+1600G>T
NM_001204298.2:c.-754+1600G>T (ZNF664) NP_001191227.1:n.-754+1600G>T
NM_001204299.3:c.-234+1600G>T NP_001191228.1:n.-234+1600G>T
NM_001347902.2:c.-234+1600G>T NP_001334831.1:n.-234+1600G>T