Canonical Allele Identifier: CA1474579563

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046673G= , CM000666.2:g.88046673G=	GRCh38
NC_000004.11:g.88967825G= , CM000666.1:g.88967825G=	GRCh37
NC_000004.10:g.89186849G=	NCBI36
NG_008604.1:g.44006G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.1351G= MANE Select	ENSP00000237596.2:p.Val451=
ENST00000237596.6:c.1351G=	ENSP00000237596.2:p.Val451=
ENST00000508588.5:c.-199+3216G=	ENSP00000427131.1:n.-199+3216G=
NM_000297.3:c.1351G=	NP_000288.1:p.Val451=
XM_011532028.1:c.1126G=	XP_011530330.1:p.Val376=
XM_011532029.1:c.631G=	XP_011530331.1:p.Val211=
XM_011532030.1:c.511G=	XP_011530332.1:p.Val171=
XR_244632.2:n.1446G=
NR_156488.1:n.1438G=
XM_011532028.2:c.1126G=	XP_011530330.1:p.Val376=
XM_011532030.2:c.511G=	XP_011530332.1:p.Val171=
NM_000297.4:c.1351G= MANE Select	NP_000288.1:p.Val451=
NR_156488.2:n.1450G=