Canonical Allele Identifier: CA1474575884

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038493T= , CM000666.2:g.88038493T=	GRCh38
NC_000004.11:g.88959645T= , CM000666.1:g.88959645T=	GRCh37
NC_000004.10:g.89178669T=	NCBI36
NG_008604.1:g.35826T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1086T= MANE Select	ENSP00000237596.2:p.Asn362=
ENST00000237596.6:c.1086T=	ENSP00000237596.2:p.Asn362=
ENST00000506367.1:n.533T=
NM_000297.3:c.1086T=	NP_000288.1:p.Asn362=
XM_011532028.1:c.1086T=	XP_011530330.1:p.Asn362=
XM_011532029.1:c.366T=	XP_011530331.1:p.Asn122=
XM_011532030.1:c.246T=	XP_011530332.1:p.Asn82=
XR_244632.2:n.1181T=
NR_156488.1:n.1173T=
XM_011532028.2:c.1086T=	XP_011530330.1:p.Asn362=
XM_011532030.2:c.246T=	XP_011530332.1:p.Asn82=
NM_000297.4:c.1086T= MANE Select	NP_000288.1:p.Asn362=
NR_156488.2:n.1185T=