Canonical Allele Identifier: CA1474587987

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065480G= , CM000666.2:g.88065480G=	GRCh38
NC_000004.11:g.88986632G= , CM000666.1:g.88986632G=	GRCh37
NC_000004.10:g.89205656G=	NCBI36
NG_008604.1:g.62813G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2225G= MANE Select	ENSP00000237596.2:p.Arg742=
ENST00000237596.6:c.2225G=	ENSP00000237596.2:p.Arg742=
ENST00000502363.1:c.479G=	ENSP00000425289.1:p.Arg160=
ENST00000508588.5:c.479G=	ENSP00000427131.1:p.Arg160=
ENST00000511337.5:n.477G=
ENST00000512858.1:n.437G=
NM_000297.3:c.2225G=	NP_000288.1:p.Arg742=
XM_011532028.1:c.2000G=	XP_011530330.1:p.Arg667=
XM_011532029.1:c.1505G=	XP_011530331.1:p.Arg502=
XM_011532030.1:c.1385G=	XP_011530332.1:p.Arg462=
NR_156488.1:n.2191G=
XM_011532028.2:c.2000G=	XP_011530330.1:p.Arg667=
XM_011532030.2:c.1385G=	XP_011530332.1:p.Arg462=
NM_000297.4:c.2225G= MANE Select	NP_000288.1:p.Arg742=
NR_156488.2:n.2203G=