Canonical Allele Identifier: CA231781409
Gene: FERRY3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4490514T>C , CM000674.2:g.4490514T>C GRCh38
NC_000012.11:g.4599680T>C , CM000674.1:g.4599680T>C GRCh37
NC_000012.10:g.4469941T>C NCBI36
NG_051648.1:g.52995A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261250.8:c.1566+8A>G MANE Select ENSP00000261250.3:n.1566+8A>G
ENST00000261250.7:c.1566+8A>G ENSP00000261250.3:n.1566+8A>G
ENST00000544258.1:c.622+8A>G ENSP00000444594.1:n.622+8A>G
ENST00000545746.5:c.1566+8A>G ENSP00000439996.1:n.1566+8A>G
NM_001304811.1:c.1566+8A>G NP_001291740.1:n.1566+8A>G
NM_020374.3:c.1566+8A>G NP_065107.1:n.1566+8A>G
XM_005253716.1:c.1437+8A>G XP_005253773.1:n.1437+8A>G
XM_011520986.1:c.1047+8A>G XP_011519288.1:n.1047+8A>G
NM_001346153.1:c.1437+8A>G NP_001333082.1:n.1437+8A>G
NM_001346155.1:c.1437+8A>G NP_001333084.1:n.1437+8A>G
NM_001346156.1:c.1047+8A>G NP_001333085.1:n.1047+8A>G
NM_001346157.1:c.918+8A>G NP_001333086.1:n.918+8A>G
NM_001352962.1:c.714+8A>G NP_001339891.1:n.714+8A>G
NR_144379.1:n.1584+8A>G
NR_144380.1:n.1257+8A>G
NR_144382.1:n.1054+8A>G
NM_020374.4:c.1566+8A>G MANE Select NP_065107.1:n.1566+8A>G
NM_001304811.2:c.1566+8A>G NP_001291740.1:n.1566+8A>G
NM_001346153.2:c.1437+8A>G NP_001333082.1:n.1437+8A>G
NM_001346155.2:c.1437+8A>G NP_001333084.1:n.1437+8A>G
NM_001346156.2:c.1047+8A>G NP_001333085.1:n.1047+8A>G
NM_001346157.2:c.918+8A>G NP_001333086.1:n.918+8A>G
NM_001352962.2:c.714+8A>G NP_001339891.1:n.714+8A>G
NR_144379.2:n.1545+8A>G
NR_144380.2:n.1218+8A>G
NR_144382.2:n.1015+8A>G