Canonical Allele Identifier: CA1474579624

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046831C= , CM000666.2:g.88046831C=	GRCh38
NC_000004.11:g.88967983C= , CM000666.1:g.88967983C=	GRCh37
NC_000004.10:g.89187007C=	NCBI36
NG_008604.1:g.44164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1509C= MANE Select	ENSP00000237596.2:p.Phe503=
ENST00000237596.6:c.1509C=	ENSP00000237596.2:p.Phe503=
ENST00000508588.5:c.-199+3374C=	ENSP00000427131.1:n.-199+3374C=
NM_000297.3:c.1509C=	NP_000288.1:p.Phe503=
XM_011532028.1:c.1284C=	XP_011530330.1:p.Phe428=
XM_011532029.1:c.789C=	XP_011530331.1:p.Phe263=
XM_011532030.1:c.669C=	XP_011530332.1:p.Phe223=
XR_244632.2:n.1604C=
NR_156488.1:n.1596C=
XM_011532028.2:c.1284C=	XP_011530330.1:p.Phe428=
XM_011532030.2:c.669C=	XP_011530332.1:p.Phe223=
NM_000297.4:c.1509C= MANE Select	NP_000288.1:p.Phe503=
NR_156488.2:n.1608C=