Canonical Allele Identifier: CA1474579612

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046809G= , CM000666.2:g.88046809G=	GRCh38
NC_000004.11:g.88967961G= , CM000666.1:g.88967961G=	GRCh37
NC_000004.10:g.89186985G=	NCBI36
NG_008604.1:g.44142G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1487G= MANE Select	ENSP00000237596.2:p.Arg496=
ENST00000237596.6:c.1487G=	ENSP00000237596.2:p.Arg496=
ENST00000508588.5:c.-199+3352G=	ENSP00000427131.1:n.-199+3352G=
NM_000297.3:c.1487G=	NP_000288.1:p.Arg496=
XM_011532028.1:c.1262G=	XP_011530330.1:p.Arg421=
XM_011532029.1:c.767G=	XP_011530331.1:p.Arg256=
XM_011532030.1:c.647G=	XP_011530332.1:p.Arg216=
XR_244632.2:n.1582G=
NR_156488.1:n.1574G=
XM_011532028.2:c.1262G=	XP_011530330.1:p.Arg421=
XM_011532030.2:c.647G=	XP_011530332.1:p.Arg216=
NM_000297.4:c.1487G= MANE Select	NP_000288.1:p.Arg496=
NR_156488.2:n.1586G=