Canonical Allele Identifier: CA1474592362

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88074903C= , CM000666.2:g.88074903C=	GRCh38
NC_000004.11:g.88996055C= , CM000666.1:g.88996055C=	GRCh37
NC_000004.10:g.89215079C=	NCBI36
NG_008604.1:g.72236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2614C= MANE Select	ENSP00000237596.2:p.Arg872=
ENST00000237596.6:c.2614C=	ENSP00000237596.2:p.Arg872=
ENST00000502363.1:c.868C=	ENSP00000425289.1:p.Arg290=
ENST00000508588.5:c.868C=	ENSP00000427131.1:p.Arg290=
ENST00000511337.5:n.866C=
ENST00000512858.1:n.1092C=
NM_000297.3:c.2614C=	NP_000288.1:p.Arg872=
XM_011532028.1:c.2389C=	XP_011530330.1:p.Arg797=
XM_011532029.1:c.1894C=	XP_011530331.1:p.Arg632=
XM_011532030.1:c.1774C=	XP_011530332.1:p.Arg592=
NR_156488.1:n.2580C=
XM_011532028.2:c.2389C=	XP_011530330.1:p.Arg797=
XM_011532030.2:c.1774C=	XP_011530332.1:p.Arg592=
NM_000297.4:c.2614C= MANE Select	NP_000288.1:p.Arg872=
NR_156488.2:n.2592C=