Canonical Allele Identifier: CA1474587989

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065482C= , CM000666.2:g.88065482C=	GRCh38
NC_000004.11:g.88986634C= , CM000666.1:g.88986634C=	GRCh37
NC_000004.10:g.89205658C=	NCBI36
NG_008604.1:g.62815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2227C= MANE Select	ENSP00000237596.2:p.Gln743=
ENST00000237596.6:c.2227C=	ENSP00000237596.2:p.Gln743=
ENST00000502363.1:c.481C=	ENSP00000425289.1:p.Gln161=
ENST00000508588.5:c.481C=	ENSP00000427131.1:p.Gln161=
ENST00000511337.5:n.479C=
ENST00000512858.1:n.439C=
NM_000297.3:c.2227C=	NP_000288.1:p.Gln743=
XM_011532028.1:c.2002C=	XP_011530330.1:p.Gln668=
XM_011532029.1:c.1507C=	XP_011530331.1:p.Gln503=
XM_011532030.1:c.1387C=	XP_011530332.1:p.Gln463=
NR_156488.1:n.2193C=
XM_011532028.2:c.2002C=	XP_011530330.1:p.Gln668=
XM_011532030.2:c.1387C=	XP_011530332.1:p.Gln463=
NM_000297.4:c.2227C= MANE Select	NP_000288.1:p.Gln743=
NR_156488.2:n.2205C=