Canonical Allele Identifier: CA1474579604

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046787G= , CM000666.2:g.88046787G=	GRCh38
NC_000004.11:g.88967939G= , CM000666.1:g.88967939G=	GRCh37
NC_000004.10:g.89186963G=	NCBI36
NG_008604.1:g.44120G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1465G= MANE Select	ENSP00000237596.2:p.Val489=
ENST00000237596.6:c.1465G=	ENSP00000237596.2:p.Val489=
ENST00000508588.5:c.-199+3330G=	ENSP00000427131.1:n.-199+3330G=
NM_000297.3:c.1465G=	NP_000288.1:p.Val489=
XM_011532028.1:c.1240G=	XP_011530330.1:p.Val414=
XM_011532029.1:c.745G=	XP_011530331.1:p.Val249=
XM_011532030.1:c.625G=	XP_011530332.1:p.Val209=
XR_244632.2:n.1560G=
NR_156488.1:n.1552G=
XM_011532028.2:c.1240G=	XP_011530330.1:p.Val414=
XM_011532030.2:c.625G=	XP_011530332.1:p.Val209=
NM_000297.4:c.1465G= MANE Select	NP_000288.1:p.Val489=
NR_156488.2:n.1564G=