Canonical Allele Identifier: CA1474575880

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038489G= , CM000666.2:g.88038489G=	GRCh38
NC_000004.11:g.88959641G= , CM000666.1:g.88959641G=	GRCh37
NC_000004.10:g.89178665G=	NCBI36
NG_008604.1:g.35822G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1082G= MANE Select	ENSP00000237596.2:p.Arg361=
ENST00000237596.6:c.1082G=	ENSP00000237596.2:p.Arg361=
ENST00000506367.1:n.529G=
NM_000297.3:c.1082G=	NP_000288.1:p.Arg361=
XM_011532028.1:c.1082G=	XP_011530330.1:p.Arg361=
XM_011532029.1:c.362G=	XP_011530331.1:p.Arg121=
XM_011532030.1:c.242G=	XP_011530332.1:p.Arg81=
XR_244632.2:n.1177G=
NR_156488.1:n.1169G=
XM_011532028.2:c.1082G=	XP_011530330.1:p.Arg361=
XM_011532030.2:c.242G=	XP_011530332.1:p.Arg81=
NM_000297.4:c.1082G= MANE Select	NP_000288.1:p.Arg361=
NR_156488.2:n.1181G=