Canonical Allele Identifier: CA1474587993

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065492A= , CM000666.2:g.88065492A=	GRCh38
NC_000004.11:g.88986644A= , CM000666.1:g.88986644A=	GRCh37
NC_000004.10:g.89205668A=	NCBI36
NG_008604.1:g.62825A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2237A= MANE Select	ENSP00000237596.2:p.Lys746=
ENST00000237596.6:c.2237A=	ENSP00000237596.2:p.Lys746=
ENST00000502363.1:c.491A=	ENSP00000425289.1:p.Lys164=
ENST00000508588.5:c.491A=	ENSP00000427131.1:p.Lys164=
ENST00000511337.5:n.489A=
ENST00000512858.1:n.449A=
NM_000297.3:c.2237A=	NP_000288.1:p.Lys746=
XM_011532028.1:c.2012A=	XP_011530330.1:p.Lys671=
XM_011532029.1:c.1517A=	XP_011530331.1:p.Lys506=
XM_011532030.1:c.1397A=	XP_011530332.1:p.Lys466=
NR_156488.1:n.2203A=
XM_011532028.2:c.2012A=	XP_011530330.1:p.Lys671=
XM_011532030.2:c.1397A=	XP_011530332.1:p.Lys466=
NM_000297.4:c.2237A= MANE Select	NP_000288.1:p.Lys746=
NR_156488.2:n.2215A=