Canonical Allele Identifier: CA1474579756

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047115T= , CM000666.2:g.88047115T=	GRCh38
NC_000004.11:g.88968267T= , CM000666.1:g.88968267T=	GRCh37
NC_000004.10:g.89187291T=	NCBI36
NG_008604.1:g.44448T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+245T= MANE Select	ENSP00000237596.2:n.1548+245T=
ENST00000237596.6:c.1548+245T=	ENSP00000237596.2:n.1548+245T=
ENST00000508588.5:c.-199+3658T=	ENSP00000427131.1:n.-199+3658T=
NM_000297.3:c.1548+245T=	NP_000288.1:n.1548+245T=
XM_011532028.1:c.1323+245T=	XP_011530330.1:n.1323+245T=
XM_011532029.1:c.828+245T=	XP_011530331.1:n.828+245T=
XM_011532030.1:c.708+245T=	XP_011530332.1:n.708+245T=
XR_244632.2:n.1643+245T=
NR_156488.1:n.1635+245T=
XM_011532028.2:c.1323+245T=	XP_011530330.1:n.1323+245T=
XM_011532030.2:c.708+245T=	XP_011530332.1:n.708+245T=
NM_000297.4:c.1548+245T= MANE Select	NP_000288.1:n.1548+245T=
NR_156488.2:n.1647+245T=