Canonical Allele Identifier: CA357626837

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88929369C>G (hg19) ; chr4:g.88008217C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008217C>G , CM000666.2:g.88008217C>G	GRCh38
NC_000004.11:g.88929369C>G , CM000666.1:g.88929369C>G	GRCh37
NC_000004.10:g.89148393C>G	NCBI36
NG_008604.1:g.5550C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.484C>G MANE Select	ENSP00000237596.2:p.Pro162Ala
ENST00000237596.6:c.484C>G	ENSP00000237596.2:p.Pro162Ala
NM_000297.3:c.484C>G	NP_000288.1:p.Pro162Ala
XM_011532028.1:c.484C>G	XP_011530330.1:p.Pro162Ala
XR_244632.2:n.579C>G
NR_156488.1:n.571C>G
XM_011532028.2:c.484C>G	XP_011530330.1:p.Pro162Ala
NM_000297.4:c.484C>G MANE Select	NP_000288.1:p.Pro162Ala
NR_156488.2:n.583C>G