Canonical Allele Identifier: CA1474579597

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046767T= , CM000666.2:g.88046767T=	GRCh38
NC_000004.11:g.88967919T= , CM000666.1:g.88967919T=	GRCh37
NC_000004.10:g.89186943T=	NCBI36
NG_008604.1:g.44100T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1445T= MANE Select	ENSP00000237596.2:p.Phe482=
ENST00000237596.6:c.1445T=	ENSP00000237596.2:p.Phe482=
ENST00000508588.5:c.-199+3310T=	ENSP00000427131.1:n.-199+3310T=
NM_000297.3:c.1445T=	NP_000288.1:p.Phe482=
XM_011532028.1:c.1220T=	XP_011530330.1:p.Phe407=
XM_011532029.1:c.725T=	XP_011530331.1:p.Phe242=
XM_011532030.1:c.605T=	XP_011530332.1:p.Phe202=
XR_244632.2:n.1540T=
NR_156488.1:n.1532T=
XM_011532028.2:c.1220T=	XP_011530330.1:p.Phe407=
XM_011532030.2:c.605T=	XP_011530332.1:p.Phe202=
NM_000297.4:c.1445T= MANE Select	NP_000288.1:p.Phe482=
NR_156488.2:n.1544T=