Canonical Allele Identifier: CA1474587991

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065486A= , CM000666.2:g.88065486A=	GRCh38
NC_000004.11:g.88986638A= , CM000666.1:g.88986638A=	GRCh37
NC_000004.10:g.89205662A=	NCBI36
NG_008604.1:g.62819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2231A= MANE Select	ENSP00000237596.2:p.Asp744=
ENST00000237596.6:c.2231A=	ENSP00000237596.2:p.Asp744=
ENST00000502363.1:c.485A=	ENSP00000425289.1:p.Asp162=
ENST00000508588.5:c.485A=	ENSP00000427131.1:p.Asp162=
ENST00000511337.5:n.483A=
ENST00000512858.1:n.443A=
NM_000297.3:c.2231A=	NP_000288.1:p.Asp744=
XM_011532028.1:c.2006A=	XP_011530330.1:p.Asp669=
XM_011532029.1:c.1511A=	XP_011530331.1:p.Asp504=
XM_011532030.1:c.1391A=	XP_011530332.1:p.Asp464=
NR_156488.1:n.2197A=
XM_011532028.2:c.2006A=	XP_011530330.1:p.Asp669=
XM_011532030.2:c.1391A=	XP_011530332.1:p.Asp464=
NM_000297.4:c.2231A= MANE Select	NP_000288.1:p.Asp744=
NR_156488.2:n.2209A=