Canonical Allele Identifier: CA357624723

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88986632G>C (hg19) ; chr4:g.88065480G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065480G>C , CM000666.2:g.88065480G>C	GRCh38
NC_000004.11:g.88986632G>C , CM000666.1:g.88986632G>C	GRCh37
NC_000004.10:g.89205656G>C	NCBI36
NG_008604.1:g.62813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2225G>C MANE Select	ENSP00000237596.2:p.Arg742Pro
ENST00000237596.6:c.2225G>C	ENSP00000237596.2:p.Arg742Pro
ENST00000502363.1:c.479G>C	ENSP00000425289.1:p.Arg160Pro
ENST00000508588.5:c.479G>C	ENSP00000427131.1:p.Arg160Pro
ENST00000511337.5:n.477G>C
ENST00000512858.1:n.437G>C
NM_000297.3:c.2225G>C	NP_000288.1:p.Arg742Pro
XM_011532028.1:c.2000G>C	XP_011530330.1:p.Arg667Pro
XM_011532029.1:c.1505G>C	XP_011530331.1:p.Arg502Pro
XM_011532030.1:c.1385G>C	XP_011530332.1:p.Arg462Pro
NR_156488.1:n.2191G>C
XM_011532028.2:c.2000G>C	XP_011530330.1:p.Arg667Pro
XM_011532030.2:c.1385G>C	XP_011530332.1:p.Arg462Pro
NM_000297.4:c.2225G>C MANE Select	NP_000288.1:p.Arg742Pro
NR_156488.2:n.2203G>C