Canonical Allele Identifier: CA1624187008
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721900G= , CM000668.2:g.42721900G= GRCh38
NC_000006.11:g.42689638G= , CM000668.1:g.42689638G= GRCh37
NC_000006.10:g.42797616G= NCBI36
NG_009176.1:g.5721C=
NG_009176.2:g.5721C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.435C= MANE Select ENSP00000230381.5:p.Asp145=
ENST00000230381.6:c.435C= ENSP00000230381.5:p.Asp145=
NM_000322.4:c.435C= NP_000313.2:p.Asp145=
XR_427834.2:n.1090C=
XR_926295.1:n.1090C=
XR_427834.4:n.1140C=
XR_926295.3:n.1140C=
NM_000322.5:c.435C= MANE Select NP_000313.2:p.Asp145=