Canonical Allele Identifier: CA1474579611

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046808C= , CM000666.2:g.88046808C=	GRCh38
NC_000004.11:g.88967960C= , CM000666.1:g.88967960C=	GRCh37
NC_000004.10:g.89186984C=	NCBI36
NG_008604.1:g.44141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1486C= MANE Select	ENSP00000237596.2:p.Arg496=
ENST00000237596.6:c.1486C=	ENSP00000237596.2:p.Arg496=
ENST00000508588.5:c.-199+3351C=	ENSP00000427131.1:n.-199+3351C=
NM_000297.3:c.1486C=	NP_000288.1:p.Arg496=
XM_011532028.1:c.1261C=	XP_011530330.1:p.Arg421=
XM_011532029.1:c.766C=	XP_011530331.1:p.Arg256=
XM_011532030.1:c.646C=	XP_011530332.1:p.Arg216=
XR_244632.2:n.1581C=
NR_156488.1:n.1573C=
XM_011532028.2:c.1261C=	XP_011530330.1:p.Arg421=
XM_011532030.2:c.646C=	XP_011530332.1:p.Arg216=
NM_000297.4:c.1486C= MANE Select	NP_000288.1:p.Arg496=
NR_156488.2:n.1585C=