Canonical Allele Identifier: CA1474588011

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065542G= , CM000666.2:g.88065542G=	GRCh38
NC_000004.11:g.88986694G= , CM000666.1:g.88986694G=	GRCh37
NC_000004.10:g.89205718G=	NCBI36
NG_008604.1:g.62875G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2240+47G= MANE Select	ENSP00000237596.2:n.2240+47G=
ENST00000237596.6:c.2240+47G=	ENSP00000237596.2:n.2240+47G=
ENST00000502363.1:c.494+47G=	ENSP00000425289.1:n.494+47G=
ENST00000508588.5:c.494+47G=	ENSP00000427131.1:n.494+47G=
ENST00000511337.5:n.492+47G=
ENST00000512858.1:n.499G=
NM_000297.3:c.2240+47G=	NP_000288.1:n.2240+47G=
XM_011532028.1:c.2015+47G=	XP_011530330.1:n.2015+47G=
XM_011532029.1:c.1520+47G=	XP_011530331.1:n.1520+47G=
XM_011532030.1:c.1400+47G=	XP_011530332.1:n.1400+47G=
NR_156488.1:n.2206+47G=
XM_011532028.2:c.2015+47G=	XP_011530330.1:n.2015+47G=
XM_011532030.2:c.1400+47G=	XP_011530332.1:n.1400+47G=
NM_000297.4:c.2240+47G= MANE Select	NP_000288.1:n.2240+47G=
NR_156488.2:n.2218+47G=