Canonical Allele Identifier: CA1474579565

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046676A= , CM000666.2:g.88046676A=	GRCh38
NC_000004.11:g.88967828A= , CM000666.1:g.88967828A=	GRCh37
NC_000004.10:g.89186852A=	NCBI36
NG_008604.1:g.44009A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.1354A= MANE Select	ENSP00000237596.2:p.Ile452=
ENST00000237596.6:c.1354A=	ENSP00000237596.2:p.Ile452=
ENST00000508588.5:c.-199+3219A=	ENSP00000427131.1:n.-199+3219A=
NM_000297.3:c.1354A=	NP_000288.1:p.Ile452=
XM_011532028.1:c.1129A=	XP_011530330.1:p.Ile377=
XM_011532029.1:c.634A=	XP_011530331.1:p.Ile212=
XM_011532030.1:c.514A=	XP_011530332.1:p.Ile172=
XR_244632.2:n.1449A=
NR_156488.1:n.1441A=
XM_011532028.2:c.1129A=	XP_011530330.1:p.Ile377=
XM_011532030.2:c.514A=	XP_011530332.1:p.Ile172=
NM_000297.4:c.1354A= MANE Select	NP_000288.1:p.Ile452=
NR_156488.2:n.1453A=