Canonical Allele Identifier: CA1474575761

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038206C= , CM000666.2:g.88038206C=	GRCh38
NC_000004.11:g.88959358C= , CM000666.1:g.88959358C=	GRCh37
NC_000004.10:g.89178382C=	NCBI36
NG_008604.1:g.35539C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.844-45C= MANE Select	ENSP00000237596.2:n.844-45C=
ENST00000237596.6:c.844-45C=	ENSP00000237596.2:n.844-45C=
ENST00000506367.1:n.291-45C=
ENST00000506727.1:n.430-45C=
NM_000297.3:c.844-45C=	NP_000288.1:n.844-45C=
XM_011532028.1:c.844-45C=	XP_011530330.1:n.844-45C=
XM_011532029.1:c.124-45C=	XP_011530331.1:n.124-45C=
XM_011532030.1:c.4-45C=	XP_011530332.1:n.4-45C=
XR_244632.2:n.939-45C=
NR_156488.1:n.931-45C=
XM_011532028.2:c.844-45C=	XP_011530330.1:n.844-45C=
XM_011532030.2:c.4-45C=	XP_011530332.1:n.4-45C=
NM_000297.4:c.844-45C= MANE Select	NP_000288.1:n.844-45C=
NR_156488.2:n.943-45C=