Canonical Allele Identifier: CA1474578078

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043325C= , CM000666.2:g.88043325C=	GRCh38
NC_000004.11:g.88964477C= , CM000666.1:g.88964477C=	GRCh37
NC_000004.10:g.89183501C=	NCBI36
NG_008604.1:g.40658C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1187C= MANE Select	ENSP00000237596.2:p.Ser396=
ENST00000237596.6:c.1187C=	ENSP00000237596.2:p.Ser396=
ENST00000506367.1:n.634C=
ENST00000508588.5:c.-331C=	ENSP00000427131.1:n.-331C=
NM_000297.3:c.1187C=	NP_000288.1:p.Ser396=
XM_011532028.1:c.1095-3317C=	XP_011530330.1:n.1095-3317C=
XM_011532029.1:c.467C=	XP_011530331.1:p.Ser156=
XM_011532030.1:c.347C=	XP_011530332.1:p.Ser116=
XR_244632.2:n.1282C=
NR_156488.1:n.1274C=
XM_011532028.2:c.1095-3317C=	XP_011530330.1:n.1095-3317C=
XM_011532030.2:c.347C=	XP_011530332.1:p.Ser116=
NM_000297.4:c.1187C= MANE Select	NP_000288.1:p.Ser396=
NR_156488.2:n.1286C=