Canonical Allele Identifier: CA2499218283
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1072932
ClinVar RCV Id: RCV001385782
dbSNP Id: rs1426763534

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721898dup , CM000668.2:g.42721898dup GRCh38
NC_000006.11:g.42689636dup , CM000668.1:g.42689636dup GRCh37
NC_000006.10:g.42797614dup NCBI36
NG_009176.1:g.5726dup
NG_009176.2:g.5726dup

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.440dup MANE Select ENSP00000230381.5:p.Gly148TrpfsTer29
ENST00000230381.6:c.440dup ENSP00000230381.5:p.Gly148TrpfsTer29
NM_000322.4:c.440dup NP_000313.2:p.Gly148TrpfsTer29
XR_427834.2:n.1095dup
XR_926295.1:n.1095dup
XR_427834.4:n.1145dup
XR_926295.3:n.1145dup
NM_000322.5:c.440dup MANE Select NP_000313.2:p.Gly148TrpfsTer29