Canonical Allele Identifier: CA1474578088

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043349C= , CM000666.2:g.88043349C=	GRCh38
NC_000004.11:g.88964501C= , CM000666.1:g.88964501C=	GRCh37
NC_000004.10:g.89183525C=	NCBI36
NG_008604.1:g.40682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1211C= MANE Select	ENSP00000237596.2:p.Ala404=
ENST00000237596.6:c.1211C=	ENSP00000237596.2:p.Ala404=
ENST00000506367.1:n.658C=
ENST00000508588.5:c.-307C=	ENSP00000427131.1:n.-307C=
NM_000297.3:c.1211C=	NP_000288.1:p.Ala404=
XM_011532028.1:c.1095-3293C=	XP_011530330.1:n.1095-3293C=
XM_011532029.1:c.491C=	XP_011530331.1:p.Ala164=
XM_011532030.1:c.371C=	XP_011530332.1:p.Ala124=
XR_244632.2:n.1306C=
NR_156488.1:n.1298C=
XM_011532028.2:c.1095-3293C=	XP_011530330.1:n.1095-3293C=
XM_011532030.2:c.371C=	XP_011530332.1:p.Ala124=
NM_000297.4:c.1211C= MANE Select	NP_000288.1:p.Ala404=
NR_156488.2:n.1310C=