Canonical Allele Identifier: CA1624186994
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721871_42721874delinsGTCT , CM000668.2:g.42721871_42721874delinsGTCT GRCh38
NC_000006.11:g.42689609_42689612delinsGTCT , CM000668.1:g.42689609_42689612delinsGTCT GRCh37
NC_000006.10:g.42797587_42797590delinsGTCT NCBI36
NG_009176.1:g.5747_5750delinsAGAC
NG_009176.2:g.5747_5750delinsAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.461_464delinsAGAC MANE Select ENSP00000230381.5:p.Lys154=
ENST00000230381.6:c.461_464delinsAGAC ENSP00000230381.5:p.Lys154=
NM_000322.4:c.461_464delinsAGAC NP_000313.2:p.Lys154=
XR_427834.2:n.1116_1119delinsAGAC
XR_926295.1:n.1116_1119delinsAGAC
XR_427834.4:n.1166_1169delinsAGAC
XR_926295.3:n.1166_1169delinsAGAC
NM_000322.5:c.461_464delinsAGAC MANE Select NP_000313.2:p.Lys154=