Canonical Allele Identifier: CA1474575879

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038488C= , CM000666.2:g.88038488C=	GRCh38
NC_000004.11:g.88959640C= , CM000666.1:g.88959640C=	GRCh37
NC_000004.10:g.89178664C=	NCBI36
NG_008604.1:g.35821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1081C= MANE Select	ENSP00000237596.2:p.Arg361=
ENST00000237596.6:c.1081C=	ENSP00000237596.2:p.Arg361=
ENST00000506367.1:n.528C=
NM_000297.3:c.1081C=	NP_000288.1:p.Arg361=
XM_011532028.1:c.1081C=	XP_011530330.1:p.Arg361=
XM_011532029.1:c.361C=	XP_011530331.1:p.Arg121=
XM_011532030.1:c.241C=	XP_011530332.1:p.Arg81=
XR_244632.2:n.1176C=
NR_156488.1:n.1168C=
XM_011532028.2:c.1081C=	XP_011530330.1:p.Arg361=
XM_011532030.2:c.241C=	XP_011530332.1:p.Arg81=
NM_000297.4:c.1081C= MANE Select	NP_000288.1:p.Arg361=
NR_156488.2:n.1180C=