Canonical Allele Identifier: CA1474579729

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047050G= , CM000666.2:g.88047050G=	GRCh38
NC_000004.11:g.88968202G= , CM000666.1:g.88968202G=	GRCh37
NC_000004.10:g.89187226G=	NCBI36
NG_008604.1:g.44383G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+180G= MANE Select	ENSP00000237596.2:n.1548+180G=
ENST00000237596.6:c.1548+180G=	ENSP00000237596.2:n.1548+180G=
ENST00000508588.5:c.-199+3593G=	ENSP00000427131.1:n.-199+3593G=
NM_000297.3:c.1548+180G=	NP_000288.1:n.1548+180G=
XM_011532028.1:c.1323+180G=	XP_011530330.1:n.1323+180G=
XM_011532029.1:c.828+180G=	XP_011530331.1:n.828+180G=
XM_011532030.1:c.708+180G=	XP_011530332.1:n.708+180G=
XR_244632.2:n.1643+180G=
NR_156488.1:n.1635+180G=
XM_011532028.2:c.1323+180G=	XP_011530330.1:n.1323+180G=
XM_011532030.2:c.708+180G=	XP_011530332.1:n.708+180G=
NM_000297.4:c.1548+180G= MANE Select	NP_000288.1:n.1548+180G=
NR_156488.2:n.1647+180G=