Canonical Allele Identifier: CA1474575839

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038381G= , CM000666.2:g.88038381G=	GRCh38
NC_000004.11:g.88959533G= , CM000666.1:g.88959533G=	GRCh37
NC_000004.10:g.89178557G=	NCBI36
NG_008604.1:g.35714G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.974G= MANE Select	ENSP00000237596.2:p.Arg325=
ENST00000237596.6:c.974G=	ENSP00000237596.2:p.Arg325=
ENST00000506367.1:n.421G=
NM_000297.3:c.974G=	NP_000288.1:p.Arg325=
XM_011532028.1:c.974G=	XP_011530330.1:p.Arg325=
XM_011532029.1:c.254G=	XP_011530331.1:p.Arg85=
XM_011532030.1:c.134G=	XP_011530332.1:p.Arg45=
XR_244632.2:n.1069G=
NR_156488.1:n.1061G=
XM_011532028.2:c.974G=	XP_011530330.1:p.Arg325=
XM_011532030.2:c.134G=	XP_011530332.1:p.Arg45=
NM_000297.4:c.974G= MANE Select	NP_000288.1:p.Arg325=
NR_156488.2:n.1073G=