Canonical Allele Identifier: CA1474575838

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038380C= , CM000666.2:g.88038380C=	GRCh38
NC_000004.11:g.88959532C= , CM000666.1:g.88959532C=	GRCh37
NC_000004.10:g.89178556C=	NCBI36
NG_008604.1:g.35713C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.973C= MANE Select	ENSP00000237596.2:p.Arg325=
ENST00000237596.6:c.973C=	ENSP00000237596.2:p.Arg325=
ENST00000506367.1:n.420C=
NM_000297.3:c.973C=	NP_000288.1:p.Arg325=
XM_011532028.1:c.973C=	XP_011530330.1:p.Arg325=
XM_011532029.1:c.253C=	XP_011530331.1:p.Arg85=
XM_011532030.1:c.133C=	XP_011530332.1:p.Arg45=
XR_244632.2:n.1068C=
NR_156488.1:n.1060C=
XM_011532028.2:c.973C=	XP_011530330.1:p.Arg325=
XM_011532030.2:c.133C=	XP_011530332.1:p.Arg45=
NM_000297.4:c.973C= MANE Select	NP_000288.1:p.Arg325=
NR_156488.2:n.1072C=