Canonical Allele Identifier: CA1474579728

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047047T= , CM000666.2:g.88047047T=	GRCh38
NC_000004.11:g.88968199T= , CM000666.1:g.88968199T=	GRCh37
NC_000004.10:g.89187223T=	NCBI36
NG_008604.1:g.44380T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+177T= MANE Select	ENSP00000237596.2:n.1548+177T=
ENST00000237596.6:c.1548+177T=	ENSP00000237596.2:n.1548+177T=
ENST00000508588.5:c.-199+3590T=	ENSP00000427131.1:n.-199+3590T=
NM_000297.3:c.1548+177T=	NP_000288.1:n.1548+177T=
XM_011532028.1:c.1323+177T=	XP_011530330.1:n.1323+177T=
XM_011532029.1:c.828+177T=	XP_011530331.1:n.828+177T=
XM_011532030.1:c.708+177T=	XP_011530332.1:n.708+177T=
XR_244632.2:n.1643+177T=
NR_156488.1:n.1635+177T=
XM_011532028.2:c.1323+177T=	XP_011530330.1:n.1323+177T=
XM_011532030.2:c.708+177T=	XP_011530332.1:n.708+177T=
NM_000297.4:c.1548+177T= MANE Select	NP_000288.1:n.1548+177T=
NR_156488.2:n.1647+177T=