Canonical Allele Identifier: CA567149497
Gene: PRPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1426763534

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.440del MANE Select ENSP00000230381.5:p.Pro147LeufsTer6
ENST00000230381.6:c.440del ENSP00000230381.5:p.Pro147LeufsTer6
NM_000322.4:c.440del NP_000313.2:p.Pro147LeufsTer6
XR_427834.2:n.1095del
XR_926295.1:n.1095del
XR_427834.4:n.1145del
XR_926295.3:n.1145del
NM_000322.5:c.440del MANE Select NP_000313.2:p.Pro147LeufsTer6