Canonical Allele Identifier: CA1474578090

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043354G= , CM000666.2:g.88043354G=	GRCh38
NC_000004.11:g.88964506G= , CM000666.1:g.88964506G=	GRCh37
NC_000004.10:g.89183530G=	NCBI36
NG_008604.1:g.40687G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.1216G= MANE Select	ENSP00000237596.2:p.Val406=
ENST00000237596.6:c.1216G=	ENSP00000237596.2:p.Val406=
ENST00000506367.1:n.663G=
ENST00000508588.5:c.-302G=	ENSP00000427131.1:n.-302G=
NM_000297.3:c.1216G=	NP_000288.1:p.Val406=
XM_011532028.1:c.1095-3288G=	XP_011530330.1:n.1095-3288G=
XM_011532029.1:c.496G=	XP_011530331.1:p.Val166=
XM_011532030.1:c.376G=	XP_011530332.1:p.Val126=
XR_244632.2:n.1311G=
NR_156488.1:n.1303G=
XM_011532028.2:c.1095-3288G=	XP_011530330.1:n.1095-3288G=
XM_011532030.2:c.376G=	XP_011530332.1:p.Val126=
NM_000297.4:c.1216G= MANE Select	NP_000288.1:p.Val406=
NR_156488.2:n.1315G=