Canonical Allele Identifier: CA378258563

Gene: PAX2

Linked Data

• ClinVar Variation Id: 155928
• ClinVar RCV Id: RCV000144050
• dbSNP Id: rs1131692055
• MyVariant Identifiers: chr10:g.102541071G>A (hg19) ; chr10:g.100781314G>A (hg38)
• PubMed: PMID:24676634

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100781314G>A , CM000672.2:g.100781314G>A	GRCh38
NC_000010.10:g.102541071G>A , CM000672.1:g.102541071G>A	GRCh37
NC_000010.9:g.102531061G>A	NCBI36
NG_008680.1:g.40604G>A
NG_008680.2:g.50606G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000707078.1:c.658G>A	ENSP00000516729.1:p.Gly220Arg
ENST00000707079.1:c.565G>A	ENSP00000516730.1:p.Gly189Arg
ENST00000355243.8:c.565G>A MANE Select	ENSP00000347385.3:p.Gly189Arg
ENST00000427256.6:c.565G>A	ENSP00000398652.2:p.Gly189Arg
ENST00000679374.1:c.547G>A	ENSP00000506041.1:p.Gly183Arg
ENST00000355243.7:c.565G>A	ENSP00000347385.2:p.Gly189Arg
ENST00000361791.7:c.562G>A	ENSP00000355069.4:p.Gly188Arg
ENST00000370296.6:c.565G>A	ENSP00000359319.3:p.Gly189Arg
ENST00000427256.5:c.565G>A	ENSP00000398652.1:p.Gly189Arg
ENST00000428433.5:c.565G>A	ENSP00000396259.1:p.Gly189Arg
ENST00000553492.5:n.286G>A
ENST00000554172.2:c.577G>A	ENSP00000452489.2:p.Gly193Arg
ENST00000554363.2:n.280G>A
NM_000278.3:c.565G>A	NP_000269.2:p.Gly189Arg
NM_001304569.1:c.658G>A	NP_001291498.1:p.Gly220Arg
NM_003987.3:c.565G>A	NP_003978.2:p.Gly189Arg
NM_003988.3:c.565G>A	NP_003979.2:p.Gly189Arg
NM_003989.3:c.565G>A	NP_003980.2:p.Gly189Arg
NM_003990.3:c.565G>A	NP_003981.2:p.Gly189Arg
NM_000278.4:c.565G>A	NP_000269.3:p.Gly189Arg
NM_003987.4:c.565G>A	NP_003978.3:p.Gly189Arg
NM_003988.4:c.565G>A	NP_003979.2:p.Gly189Arg
NM_003989.4:c.565G>A	NP_003980.3:p.Gly189Arg
NM_003990.4:c.565G>A	NP_003981.3:p.Gly189Arg
NM_000278.5:c.565G>A MANE Select	NP_000269.3:p.Gly189Arg
NM_001304569.2:c.658G>A	NP_001291498.1:p.Gly220Arg
NM_003987.5:c.565G>A	NP_003978.3:p.Gly189Arg
NM_003988.5:c.565G>A	NP_003979.2:p.Gly189Arg
NM_003989.5:c.565G>A	NP_003980.3:p.Gly189Arg
NM_003990.5:c.565G>A	NP_003981.3:p.Gly189Arg