Canonical Allele Identifier: CA1474575813

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038323C= , CM000666.2:g.88038323C=	GRCh38
NC_000004.11:g.88959475C= , CM000666.1:g.88959475C=	GRCh37
NC_000004.10:g.89178499C=	NCBI36
NG_008604.1:g.35656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.916C= MANE Select	ENSP00000237596.2:p.Arg306=
ENST00000237596.6:c.916C=	ENSP00000237596.2:p.Arg306=
ENST00000506367.1:n.363C=
ENST00000506727.1:n.502C=
NM_000297.3:c.916C=	NP_000288.1:p.Arg306=
XM_011532028.1:c.916C=	XP_011530330.1:p.Arg306=
XM_011532029.1:c.196C=	XP_011530331.1:p.Arg66=
XM_011532030.1:c.76C=	XP_011530332.1:p.Arg26=
XR_244632.2:n.1011C=
NR_156488.1:n.1003C=
XM_011532028.2:c.916C=	XP_011530330.1:p.Arg306=
XM_011532030.2:c.76C=	XP_011530332.1:p.Arg26=
NM_000297.4:c.916C= MANE Select	NP_000288.1:p.Arg306=
NR_156488.2:n.1015C=