Canonical Allele Identifier: CA1474575831

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038365C= , CM000666.2:g.88038365C=	GRCh38
NC_000004.11:g.88959517C= , CM000666.1:g.88959517C=	GRCh37
NC_000004.10:g.89178541C=	NCBI36
NG_008604.1:g.35698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.958C= MANE Select	ENSP00000237596.2:p.Arg320=
ENST00000237596.6:c.958C=	ENSP00000237596.2:p.Arg320=
ENST00000506367.1:n.405C=
ENST00000506727.1:n.544C=
NM_000297.3:c.958C=	NP_000288.1:p.Arg320=
XM_011532028.1:c.958C=	XP_011530330.1:p.Arg320=
XM_011532029.1:c.238C=	XP_011530331.1:p.Arg80=
XM_011532030.1:c.118C=	XP_011530332.1:p.Arg40=
XR_244632.2:n.1053C=
NR_156488.1:n.1045C=
XM_011532028.2:c.958C=	XP_011530330.1:p.Arg320=
XM_011532030.2:c.118C=	XP_011530332.1:p.Arg40=
NM_000297.4:c.958C= MANE Select	NP_000288.1:p.Arg320=
NR_156488.2:n.1057C=