Canonical Allele Identifier: CA1474579642

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046875G= , CM000666.2:g.88046875G=	GRCh38
NC_000004.11:g.88968027G= , CM000666.1:g.88968027G=	GRCh37
NC_000004.10:g.89187051G=	NCBI36
NG_008604.1:g.44208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+5G= MANE Select	ENSP00000237596.2:n.1548+5G=
ENST00000237596.6:c.1548+5G=	ENSP00000237596.2:n.1548+5G=
ENST00000508588.5:c.-199+3418G=	ENSP00000427131.1:n.-199+3418G=
NM_000297.3:c.1548+5G=	NP_000288.1:n.1548+5G=
XM_011532028.1:c.1323+5G=	XP_011530330.1:n.1323+5G=
XM_011532029.1:c.828+5G=	XP_011530331.1:n.828+5G=
XM_011532030.1:c.708+5G=	XP_011530332.1:n.708+5G=
XR_244632.2:n.1643+5G=
NR_156488.1:n.1635+5G=
XM_011532028.2:c.1323+5G=	XP_011530330.1:n.1323+5G=
XM_011532030.2:c.708+5G=	XP_011530332.1:n.708+5G=
NM_000297.4:c.1548+5G= MANE Select	NP_000288.1:n.1548+5G=
NR_156488.2:n.1647+5G=