Canonical Allele Identifier: CA2695206298
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721976_42721985del , CM000668.2:g.42721976_42721985del GRCh38
NC_000006.11:g.42689714_42689723del , CM000668.1:g.42689714_42689723del GRCh37
NC_000006.10:g.42797692_42797701del NCBI36
NG_009176.1:g.5642_5651del
NG_009176.2:g.5642_5651del

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.356_365del MANE Select ENSP00000230381.5:p.Cys119PhefsTer17
ENST00000230381.6:c.356_365del ENSP00000230381.5:p.Cys119PhefsTer17
NM_000322.4:c.356_365del NP_000313.2:p.Cys119PhefsTer17
XR_427834.2:n.1011_1020del
XR_926295.1:n.1011_1020del
XR_427834.4:n.1061_1070del
XR_926295.3:n.1061_1070del
NM_000322.5:c.356_365del MANE Select NP_000313.2:p.Cys119PhefsTer17