Canonical Allele Identifier: CA1139659527
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 958838
dbSNP Id: rs1761913253

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722024_42722027del , CM000668.2:g.42722024_42722027del GRCh38
NC_000006.11:g.42689762_42689765del , CM000668.1:g.42689762_42689765del GRCh37
NC_000006.10:g.42797740_42797743del NCBI36
NG_009176.1:g.5596_5599del
NG_009176.2:g.5596_5599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.310_313del MANE Select ENSP00000230381.5:p.Ile104ValfsTer?
ENST00000230381.6:c.310_313del ENSP00000230381.5:p.Ile104ValfsTer?
NM_000322.4:c.310_313del NP_000313.2:p.Ile104ValfsTer?
XR_427834.2:n.965_968del
XR_926295.1:n.965_968del
XR_427834.4:n.1015_1018del
XR_926295.3:n.1015_1018del
NM_000322.5:c.310_313del MANE Select NP_000313.2:p.Ile104ValfsTer?