Canonical Allele Identifier: CA1474579559

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046668G= , CM000666.2:g.88046668G=	GRCh38
NC_000004.11:g.88967820G= , CM000666.1:g.88967820G=	GRCh37
NC_000004.10:g.89186844G=	NCBI36
NG_008604.1:g.44001G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.1346G= MANE Select	ENSP00000237596.2:p.Gly449=
ENST00000237596.6:c.1346G=	ENSP00000237596.2:p.Gly449=
ENST00000508588.5:c.-199+3211G=	ENSP00000427131.1:n.-199+3211G=
NM_000297.3:c.1346G=	NP_000288.1:p.Gly449=
XM_011532028.1:c.1121G=	XP_011530330.1:p.Gly374=
XM_011532029.1:c.626G=	XP_011530331.1:p.Gly209=
XM_011532030.1:c.506G=	XP_011530332.1:p.Gly169=
XR_244632.2:n.1441G=
NR_156488.1:n.1433G=
XM_011532028.2:c.1121G=	XP_011530330.1:p.Gly374=
XM_011532030.2:c.506G=	XP_011530332.1:p.Gly169=
NM_000297.4:c.1346G= MANE Select	NP_000288.1:p.Gly449=
NR_156488.2:n.1445G=