Canonical Allele Identifier: CA1474579603

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046785T= , CM000666.2:g.88046785T=	GRCh38
NC_000004.11:g.88967937T= , CM000666.1:g.88967937T=	GRCh37
NC_000004.10:g.89186961T=	NCBI36
NG_008604.1:g.44118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1463T= MANE Select	ENSP00000237596.2:p.Val488=
ENST00000237596.6:c.1463T=	ENSP00000237596.2:p.Val488=
ENST00000508588.5:c.-199+3328T=	ENSP00000427131.1:n.-199+3328T=
NM_000297.3:c.1463T=	NP_000288.1:p.Val488=
XM_011532028.1:c.1238T=	XP_011530330.1:p.Val413=
XM_011532029.1:c.743T=	XP_011530331.1:p.Val248=
XM_011532030.1:c.623T=	XP_011530332.1:p.Val208=
XR_244632.2:n.1558T=
NR_156488.1:n.1550T=
XM_011532028.2:c.1238T=	XP_011530330.1:p.Val413=
XM_011532030.2:c.623T=	XP_011530332.1:p.Val208=
NM_000297.4:c.1463T= MANE Select	NP_000288.1:p.Val488=
NR_156488.2:n.1562T=