Canonical Allele Identifier: CA1474579666

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046907T= , CM000666.2:g.88046907T=	GRCh38
NC_000004.11:g.88968059T= , CM000666.1:g.88968059T=	GRCh37
NC_000004.10:g.89187083T=	NCBI36
NG_008604.1:g.44240T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+37T= MANE Select	ENSP00000237596.2:n.1548+37T=
ENST00000237596.6:c.1548+37T=	ENSP00000237596.2:n.1548+37T=
ENST00000508588.5:c.-199+3450T=	ENSP00000427131.1:n.-199+3450T=
NM_000297.3:c.1548+37T=	NP_000288.1:n.1548+37T=
XM_011532028.1:c.1323+37T=	XP_011530330.1:n.1323+37T=
XM_011532029.1:c.828+37T=	XP_011530331.1:n.828+37T=
XM_011532030.1:c.708+37T=	XP_011530332.1:n.708+37T=
XR_244632.2:n.1643+37T=
NR_156488.1:n.1635+37T=
XM_011532028.2:c.1323+37T=	XP_011530330.1:n.1323+37T=
XM_011532030.2:c.708+37T=	XP_011530332.1:n.708+37T=
NM_000297.4:c.1548+37T= MANE Select	NP_000288.1:n.1548+37T=
NR_156488.2:n.1647+37T=