Canonical Allele Identifier: CA1474575835

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038372G= , CM000666.2:g.88038372G=	GRCh38
NC_000004.11:g.88959524G= , CM000666.1:g.88959524G=	GRCh37
NC_000004.10:g.89178548G=	NCBI36
NG_008604.1:g.35705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.965G= MANE Select	ENSP00000237596.2:p.Arg322=
ENST00000237596.6:c.965G=	ENSP00000237596.2:p.Arg322=
ENST00000506367.1:n.412G=
NM_000297.3:c.965G=	NP_000288.1:p.Arg322=
XM_011532028.1:c.965G=	XP_011530330.1:p.Arg322=
XM_011532029.1:c.245G=	XP_011530331.1:p.Arg82=
XM_011532030.1:c.125G=	XP_011530332.1:p.Arg42=
XR_244632.2:n.1060G=
NR_156488.1:n.1052G=
XM_011532028.2:c.965G=	XP_011530330.1:p.Arg322=
XM_011532030.2:c.125G=	XP_011530332.1:p.Arg42=
NM_000297.4:c.965G= MANE Select	NP_000288.1:p.Arg322=
NR_156488.2:n.1064G=