Canonical Allele Identifier: CA1624187191
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722303T= , CM000668.2:g.42722303T= GRCh38
NC_000006.11:g.42690041T= , CM000668.1:g.42690041T= GRCh37
NC_000006.10:g.42798019T= NCBI36
NG_009176.1:g.5318A=
NG_009176.2:g.5318A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.32A= MANE Select ENSP00000230381.5:p.Lys11=
ENST00000230381.6:c.32A= ENSP00000230381.5:p.Lys11=
NM_000322.4:c.32A= NP_000313.2:p.Lys11=
XR_427834.2:n.687A=
XR_926295.1:n.687A=
XR_427834.4:n.737A=
XR_926295.3:n.737A=
NM_000322.5:c.32A= MANE Select NP_000313.2:p.Lys11=