Canonical Allele Identifier: CA1624187200
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722322T= , CM000668.2:g.42722322T= GRCh38
NC_000006.11:g.42690060T= , CM000668.1:g.42690060T= GRCh37
NC_000006.10:g.42798038T= NCBI36
NG_009176.1:g.5299A=
NG_009176.2:g.5299A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.13A= MANE Select ENSP00000230381.5:p.Lys5=
ENST00000230381.6:c.13A= ENSP00000230381.5:p.Lys5=
NM_000322.4:c.13A= NP_000313.2:p.Lys5=
XR_427834.2:n.668A=
XR_926295.1:n.668A=
XR_427834.4:n.718A=
XR_926295.3:n.718A=
NM_000322.5:c.13A= MANE Select NP_000313.2:p.Lys5=