Canonical Allele Identifier: CA1474579626

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046835A= , CM000666.2:g.88046835A=	GRCh38
NC_000004.11:g.88967987A= , CM000666.1:g.88967987A=	GRCh37
NC_000004.10:g.89187011A=	NCBI36
NG_008604.1:g.44168A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1513A= MANE Select	ENSP00000237596.2:p.Ser505=
ENST00000237596.6:c.1513A=	ENSP00000237596.2:p.Ser505=
ENST00000508588.5:c.-199+3378A=	ENSP00000427131.1:n.-199+3378A=
NM_000297.3:c.1513A=	NP_000288.1:p.Ser505=
XM_011532028.1:c.1288A=	XP_011530330.1:p.Ser430=
XM_011532029.1:c.793A=	XP_011530331.1:p.Ser265=
XM_011532030.1:c.673A=	XP_011530332.1:p.Ser225=
XR_244632.2:n.1608A=
NR_156488.1:n.1600A=
XM_011532028.2:c.1288A=	XP_011530330.1:p.Ser430=
XM_011532030.2:c.673A=	XP_011530332.1:p.Ser225=
NM_000297.4:c.1513A= MANE Select	NP_000288.1:p.Ser505=
NR_156488.2:n.1612A=