Canonical Allele Identifier: CA1624187206

Gene: PRPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42722334T= , CM000668.2:g.42722334T=	GRCh38
NC_000006.11:g.42690072T= , CM000668.1:g.42690072T=	GRCh37
NC_000006.10:g.42798050T=	NCBI36
NG_009176.1:g.5287A=
NG_009176.2:g.5287A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.1A= MANE Select	ENSP00000230381.5:p.Met1=
ENST00000230381.6:c.1A=	ENSP00000230381.5:p.Met1=
NM_000322.4:c.1A=	NP_000313.2:p.Met1=
XR_427834.2:n.656A=
XR_926295.1:n.656A=
XR_427834.4:n.706A=
XR_926295.3:n.706A=
NM_000322.5:c.1A= MANE Select	NP_000313.2:p.Met1=