Canonical Allele Identifier: CA1474579751

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047103G= , CM000666.2:g.88047103G=	GRCh38
NC_000004.11:g.88968255G= , CM000666.1:g.88968255G=	GRCh37
NC_000004.10:g.89187279G=	NCBI36
NG_008604.1:g.44436G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+233G= MANE Select	ENSP00000237596.2:n.1548+233G=
ENST00000237596.6:c.1548+233G=	ENSP00000237596.2:n.1548+233G=
ENST00000508588.5:c.-199+3646G=	ENSP00000427131.1:n.-199+3646G=
NM_000297.3:c.1548+233G=	NP_000288.1:n.1548+233G=
XM_011532028.1:c.1323+233G=	XP_011530330.1:n.1323+233G=
XM_011532029.1:c.828+233G=	XP_011530331.1:n.828+233G=
XM_011532030.1:c.708+233G=	XP_011530332.1:n.708+233G=
XR_244632.2:n.1643+233G=
NR_156488.1:n.1635+233G=
XM_011532028.2:c.1323+233G=	XP_011530330.1:n.1323+233G=
XM_011532030.2:c.708+233G=	XP_011530332.1:n.708+233G=
NM_000297.4:c.1548+233G= MANE Select	NP_000288.1:n.1548+233G=
NR_156488.2:n.1647+233G=