Canonical Allele Identifier: CA1474575769

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038224T= , CM000666.2:g.88038224T=	GRCh38
NC_000004.11:g.88959376T= , CM000666.1:g.88959376T=	GRCh37
NC_000004.10:g.89178400T=	NCBI36
NG_008604.1:g.35557T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.844-27T= MANE Select	ENSP00000237596.2:n.844-27T=
ENST00000237596.6:c.844-27T=	ENSP00000237596.2:n.844-27T=
ENST00000506367.1:n.291-27T=
ENST00000506727.1:n.430-27T=
NM_000297.3:c.844-27T=	NP_000288.1:n.844-27T=
XM_011532028.1:c.844-27T=	XP_011530330.1:n.844-27T=
XM_011532029.1:c.124-27T=	XP_011530331.1:n.124-27T=
XM_011532030.1:c.4-27T=	XP_011530332.1:n.4-27T=
XR_244632.2:n.939-27T=
NR_156488.1:n.931-27T=
XM_011532028.2:c.844-27T=	XP_011530330.1:n.844-27T=
XM_011532030.2:c.4-27T=	XP_011530332.1:n.4-27T=
NM_000297.4:c.844-27T= MANE Select	NP_000288.1:n.844-27T=
NR_156488.2:n.943-27T=