Canonical Allele Identifier: CA1474579627

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046836G= , CM000666.2:g.88046836G=	GRCh38
NC_000004.11:g.88967988G= , CM000666.1:g.88967988G=	GRCh37
NC_000004.10:g.89187012G=	NCBI36
NG_008604.1:g.44169G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1514G= MANE Select	ENSP00000237596.2:p.Ser505=
ENST00000237596.6:c.1514G=	ENSP00000237596.2:p.Ser505=
ENST00000508588.5:c.-199+3379G=	ENSP00000427131.1:n.-199+3379G=
NM_000297.3:c.1514G=	NP_000288.1:p.Ser505=
XM_011532028.1:c.1289G=	XP_011530330.1:p.Ser430=
XM_011532029.1:c.794G=	XP_011530331.1:p.Ser265=
XM_011532030.1:c.674G=	XP_011530332.1:p.Ser225=
XR_244632.2:n.1609G=
NR_156488.1:n.1601G=
XM_011532028.2:c.1289G=	XP_011530330.1:p.Ser430=
XM_011532030.2:c.674G=	XP_011530332.1:p.Ser225=
NM_000297.4:c.1514G= MANE Select	NP_000288.1:p.Ser505=
NR_156488.2:n.1613G=