Canonical Allele Identifier: CA1474579562

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046672T= , CM000666.2:g.88046672T=	GRCh38
NC_000004.11:g.88967824T= , CM000666.1:g.88967824T=	GRCh37
NC_000004.10:g.89186848T=	NCBI36
NG_008604.1:g.44005T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.1350T= MANE Select	ENSP00000237596.2:p.Gly450=
ENST00000237596.6:c.1350T=	ENSP00000237596.2:p.Gly450=
ENST00000508588.5:c.-199+3215T=	ENSP00000427131.1:n.-199+3215T=
NM_000297.3:c.1350T=	NP_000288.1:p.Gly450=
XM_011532028.1:c.1125T=	XP_011530330.1:p.Gly375=
XM_011532029.1:c.630T=	XP_011530331.1:p.Gly210=
XM_011532030.1:c.510T=	XP_011530332.1:p.Gly170=
XR_244632.2:n.1445T=
NR_156488.1:n.1437T=
XM_011532028.2:c.1125T=	XP_011530330.1:p.Gly375=
XM_011532030.2:c.510T=	XP_011530332.1:p.Gly170=
NM_000297.4:c.1350T= MANE Select	NP_000288.1:p.Gly450=
NR_156488.2:n.1449T=