Canonical Allele Identifier: CA1474575797

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038282A= , CM000666.2:g.88038282A=	GRCh38
NC_000004.11:g.88959434A= , CM000666.1:g.88959434A=	GRCh37
NC_000004.10:g.89178458A=	NCBI36
NG_008604.1:g.35615A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.875A= MANE Select	ENSP00000237596.2:p.Tyr292=
ENST00000237596.6:c.875A=	ENSP00000237596.2:p.Tyr292=
ENST00000506367.1:n.322A=
ENST00000506727.1:n.461A=
NM_000297.3:c.875A=	NP_000288.1:p.Tyr292=
XM_011532028.1:c.875A=	XP_011530330.1:p.Tyr292=
XM_011532029.1:c.155A=	XP_011530331.1:p.Tyr52=
XM_011532030.1:c.35A=	XP_011530332.1:p.Tyr12=
XR_244632.2:n.970A=
NR_156488.1:n.962A=
XM_011532028.2:c.875A=	XP_011530330.1:p.Tyr292=
XM_011532030.2:c.35A=	XP_011530332.1:p.Tyr12=
NM_000297.4:c.875A= MANE Select	NP_000288.1:p.Tyr292=
NR_156488.2:n.974A=