Canonical Allele Identifier: CA1474589086

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88067946C= , CM000666.2:g.88067946C=	GRCh38
NC_000004.11:g.88989098C= , CM000666.1:g.88989098C=	GRCh37
NC_000004.10:g.89208122C=	NCBI36
NG_008604.1:g.65279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2407C= MANE Select	ENSP00000237596.2:p.Arg803=
ENST00000237596.6:c.2407C=	ENSP00000237596.2:p.Arg803=
ENST00000502363.1:c.661C=	ENSP00000425289.1:p.Arg221=
ENST00000508588.5:c.661C=	ENSP00000427131.1:p.Arg221=
ENST00000511337.5:n.659C=
ENST00000512858.1:n.885C=
NM_000297.3:c.2407C=	NP_000288.1:p.Arg803=
XM_011532028.1:c.2182C=	XP_011530330.1:p.Arg728=
XM_011532029.1:c.1687C=	XP_011530331.1:p.Arg563=
XM_011532030.1:c.1567C=	XP_011530332.1:p.Arg523=
NR_156488.1:n.2373C=
XM_011532028.2:c.2182C=	XP_011530330.1:p.Arg728=
XM_011532030.2:c.1567C=	XP_011530332.1:p.Arg523=
NM_000297.4:c.2407C= MANE Select	NP_000288.1:p.Arg803=
NR_156488.2:n.2385C=