Canonical Allele Identifier: CA233171

Gene: PAX2

Linked Data

• ClinVar Variation Id: 156296
• ClinVar RCV Id: RCV000014815 ; RCV000144380
• dbSNP Id: rs75399846
• MyVariant Identifiers: chr10:g.102566276C>T (hg19) ; chr10:g.100806519C>T (hg38)
• PubMed: PMID:11461952 ; PMID:22213154

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100806519C>T , CM000672.2:g.100806519C>T	GRCh38
NC_000010.10:g.102566276C>T , CM000672.1:g.102566276C>T	GRCh37
NC_000010.9:g.102556266C>T	NCBI36
NG_008680.1:g.65809C>T
NG_008680.2:g.75811C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707078.1:c.799C>T	ENSP00000516729.1:p.Gln267Ter
ENST00000707079.1:c.775C>T	ENSP00000516730.1:p.Gln259Ter
ENST00000355243.8:c.706C>T MANE Select	ENSP00000347385.3:p.Gln236Ter
ENST00000427256.6:c.706C>T	ENSP00000398652.2:p.Gln236Ter
ENST00000679374.1:c.688C>T	ENSP00000506041.1:p.Gln230Ter
ENST00000355243.7:c.706C>T	ENSP00000347385.2:p.Gln236Ter
ENST00000361791.7:c.703C>T	ENSP00000355069.4:p.Gln235Ter
ENST00000370296.6:c.706C>T	ENSP00000359319.3:p.Gln236Ter
ENST00000428433.5:c.775C>T	ENSP00000396259.1:p.Gln259Ter
ENST00000553492.5:n.427C>T
ENST00000554172.2:c.694C>T	ENSP00000452489.2:p.Gln232Ter
ENST00000554363.2:n.421C>T
NM_000278.3:c.706C>T	NP_000269.2:p.Gln236Ter
NM_001304569.1:c.799C>T	NP_001291498.1:p.Gln267Ter
NM_003987.3:c.775C>T	NP_003978.2:p.Gln259Ter
NM_003988.3:c.706C>T	NP_003979.2:p.Gln236Ter
NM_003989.3:c.706C>T	NP_003980.2:p.Gln236Ter
NM_003990.3:c.775C>T	NP_003981.2:p.Gln259Ter
NM_000278.4:c.706C>T	NP_000269.3:p.Gln236Ter
NM_003987.4:c.775C>T	NP_003978.3:p.Gln259Ter
NM_003988.4:c.706C>T	NP_003979.2:p.Gln236Ter
NM_003989.4:c.706C>T	NP_003980.3:p.Gln236Ter
NM_003990.4:c.775C>T	NP_003981.3:p.Gln259Ter
NM_000278.5:c.706C>T MANE Select	NP_000269.3:p.Gln236Ter
NM_001304569.2:c.799C>T	NP_001291498.1:p.Gln267Ter
NM_003987.5:c.775C>T	NP_003978.3:p.Gln259Ter
NM_003988.5:c.706C>T	NP_003979.2:p.Gln236Ter
NM_003989.5:c.706C>T	NP_003980.3:p.Gln236Ter
NM_003990.5:c.775C>T	NP_003981.3:p.Gln259Ter