Canonical Allele Identifier: CA1474575751

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038190G= , CM000666.2:g.88038190G=	GRCh38
NC_000004.11:g.88959342G= , CM000666.1:g.88959342G=	GRCh37
NC_000004.10:g.89178366G=	NCBI36
NG_008604.1:g.35523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.844-61G= MANE Select	ENSP00000237596.2:n.844-61G=
ENST00000237596.6:c.844-61G=	ENSP00000237596.2:n.844-61G=
ENST00000506367.1:n.291-61G=
ENST00000506727.1:n.430-61G=
NM_000297.3:c.844-61G=	NP_000288.1:n.844-61G=
XM_011532028.1:c.844-61G=	XP_011530330.1:n.844-61G=
XM_011532029.1:c.124-61G=	XP_011530331.1:n.124-61G=
XM_011532030.1:c.4-61G=	XP_011530332.1:n.4-61G=
XR_244632.2:n.939-61G=
NR_156488.1:n.931-61G=
XM_011532028.2:c.844-61G=	XP_011530330.1:n.844-61G=
XM_011532030.2:c.4-61G=	XP_011530332.1:n.4-61G=
NM_000297.4:c.844-61G= MANE Select	NP_000288.1:n.844-61G=
NR_156488.2:n.943-61G=