Canonical Allele Identifier: CA1474579610

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046804A= , CM000666.2:g.88046804A=	GRCh38
NC_000004.11:g.88967956A= , CM000666.1:g.88967956A=	GRCh37
NC_000004.10:g.89186980A=	NCBI36
NG_008604.1:g.44137A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1482A= MANE Select	ENSP00000237596.2:p.Glu494=
ENST00000237596.6:c.1482A=	ENSP00000237596.2:p.Glu494=
ENST00000508588.5:c.-199+3347A=	ENSP00000427131.1:n.-199+3347A=
NM_000297.3:c.1482A=	NP_000288.1:p.Glu494=
XM_011532028.1:c.1257A=	XP_011530330.1:p.Glu419=
XM_011532029.1:c.762A=	XP_011530331.1:p.Glu254=
XM_011532030.1:c.642A=	XP_011530332.1:p.Glu214=
XR_244632.2:n.1577A=
NR_156488.1:n.1569A=
XM_011532028.2:c.1257A=	XP_011530330.1:p.Glu419=
XM_011532030.2:c.642A=	XP_011530332.1:p.Glu214=
NM_000297.4:c.1482A= MANE Select	NP_000288.1:p.Glu494=
NR_156488.2:n.1581A=