Canonical Allele Identifier: CA357619493

Gene: PKD2

Linked Data

• dbSNP Id: rs1727790231
• MyVariant Identifiers: chr4:g.88967947G>C (hg19) ; chr4:g.88046795G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046795G>C , CM000666.2:g.88046795G>C	GRCh38
NC_000004.11:g.88967947G>C , CM000666.1:g.88967947G>C	GRCh37
NC_000004.10:g.89186971G>C	NCBI36
NG_008604.1:g.44128G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1473G>C MANE Select	ENSP00000237596.2:p.Glu491Asp
ENST00000237596.6:c.1473G>C	ENSP00000237596.2:p.Glu491Asp
ENST00000508588.5:c.-199+3338G>C	ENSP00000427131.1:n.-199+3338G>C
NM_000297.3:c.1473G>C	NP_000288.1:p.Glu491Asp
XM_011532028.1:c.1248G>C	XP_011530330.1:p.Glu416Asp
XM_011532029.1:c.753G>C	XP_011530331.1:p.Glu251Asp
XM_011532030.1:c.633G>C	XP_011530332.1:p.Glu211Asp
XR_244632.2:n.1568G>C
NR_156488.1:n.1560G>C
XM_011532028.2:c.1248G>C	XP_011530330.1:p.Glu416Asp
XM_011532030.2:c.633G>C	XP_011530332.1:p.Glu211Asp
NM_000297.4:c.1473G>C MANE Select	NP_000288.1:p.Glu491Asp
NR_156488.2:n.1572G>C