Canonical Allele Identifier: CA1474575802

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038304C= , CM000666.2:g.88038304C=	GRCh38
NC_000004.11:g.88959456C= , CM000666.1:g.88959456C=	GRCh37
NC_000004.10:g.89178480C=	NCBI36
NG_008604.1:g.35637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.897C= MANE Select	ENSP00000237596.2:p.Asn299=
ENST00000237596.6:c.897C=	ENSP00000237596.2:p.Asn299=
ENST00000506367.1:n.344C=
ENST00000506727.1:n.483C=
NM_000297.3:c.897C=	NP_000288.1:p.Asn299=
XM_011532028.1:c.897C=	XP_011530330.1:p.Asn299=
XM_011532029.1:c.177C=	XP_011530331.1:p.Asn59=
XM_011532030.1:c.57C=	XP_011530332.1:p.Asn19=
XR_244632.2:n.992C=
NR_156488.1:n.984C=
XM_011532028.2:c.897C=	XP_011530330.1:p.Asn299=
XM_011532030.2:c.57C=	XP_011530332.1:p.Asn19=
NM_000297.4:c.897C= MANE Select	NP_000288.1:p.Asn299=
NR_156488.2:n.996C=