Canonical Allele Identifier: CA1624187072

Gene: PRPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42722043G= , CM000668.2:g.42722043G=	GRCh38
NC_000006.11:g.42689781G= , CM000668.1:g.42689781G=	GRCh37
NC_000006.10:g.42797759G=	NCBI36
NG_009176.1:g.5578C=
NG_009176.2:g.5578C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.292C= MANE Select	ENSP00000230381.5:p.Leu98=
ENST00000230381.6:c.292C=	ENSP00000230381.5:p.Leu98=
NM_000322.4:c.292C=	NP_000313.2:p.Leu98=
XR_427834.2:n.947C=
XR_926295.1:n.947C=
XR_427834.4:n.997C=
XR_926295.3:n.997C=
NM_000322.5:c.292C= MANE Select	NP_000313.2:p.Leu98=