Canonical Allele Identifier: CA357624742

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88986640C>G (hg19) ; chr4:g.88065488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065488C>G , CM000666.2:g.88065488C>G	GRCh38
NC_000004.11:g.88986640C>G , CM000666.1:g.88986640C>G	GRCh37
NC_000004.10:g.89205664C>G	NCBI36
NG_008604.1:g.62821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2233C>G MANE Select	ENSP00000237596.2:p.Leu745Val
ENST00000237596.6:c.2233C>G	ENSP00000237596.2:p.Leu745Val
ENST00000502363.1:c.487C>G	ENSP00000425289.1:p.Leu163Val
ENST00000508588.5:c.487C>G	ENSP00000427131.1:p.Leu163Val
ENST00000511337.5:n.485C>G
ENST00000512858.1:n.445C>G
NM_000297.3:c.2233C>G	NP_000288.1:p.Leu745Val
XM_011532028.1:c.2008C>G	XP_011530330.1:p.Leu670Val
XM_011532029.1:c.1513C>G	XP_011530331.1:p.Leu505Val
XM_011532030.1:c.1393C>G	XP_011530332.1:p.Leu465Val
NR_156488.1:n.2199C>G
XM_011532028.2:c.2008C>G	XP_011530330.1:p.Leu670Val
XM_011532030.2:c.1393C>G	XP_011530332.1:p.Leu465Val
NM_000297.4:c.2233C>G MANE Select	NP_000288.1:p.Leu745Val
NR_156488.2:n.2211C>G