Canonical Allele Identifier: CA1474575842

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038391T= , CM000666.2:g.88038391T=	GRCh38
NC_000004.11:g.88959543T= , CM000666.1:g.88959543T=	GRCh37
NC_000004.10:g.89178567T=	NCBI36
NG_008604.1:g.35724T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.984T= MANE Select	ENSP00000237596.2:p.Asn328=
ENST00000237596.6:c.984T=	ENSP00000237596.2:p.Asn328=
ENST00000506367.1:n.431T=
NM_000297.3:c.984T=	NP_000288.1:p.Asn328=
XM_011532028.1:c.984T=	XP_011530330.1:p.Asn328=
XM_011532029.1:c.264T=	XP_011530331.1:p.Asn88=
XM_011532030.1:c.144T=	XP_011530332.1:p.Asn48=
XR_244632.2:n.1079T=
NR_156488.1:n.1071T=
XM_011532028.2:c.984T=	XP_011530330.1:p.Asn328=
XM_011532030.2:c.144T=	XP_011530332.1:p.Asn48=
NM_000297.4:c.984T= MANE Select	NP_000288.1:p.Asn328=
NR_156488.2:n.1083T=