Canonical Allele Identifier: CA471216030
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1137804
ClinVar RCV Id: RCV001473934
dbSNP Id: rs2133833930
MyVariant Identifiers: chr10:g.102509618C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100749861C>T , CM000672.2:g.100749861C>T GRCh38
NC_000010.10:g.102509618C>T , CM000672.1:g.102509618C>T GRCh37
NC_000010.9:g.102499608C>T NCBI36
NG_008680.1:g.9151C>T
NG_008680.2:g.19153C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707078.1:c.252C>T ENSP00000516729.1:p.Asp84=
ENST00000707079.1:c.159C>T ENSP00000516730.1:p.Asp53=
ENST00000355243.8:c.159C>T MANE Select ENSP00000347385.3:p.Asp53=
ENST00000427256.6:c.159C>T ENSP00000398652.2:p.Asp53=
ENST00000679374.1:c.141C>T ENSP00000506041.1:p.Asp47=
ENST00000355243.7:c.159C>T ENSP00000347385.2:p.Asp53=
ENST00000361791.7:c.156C>T ENSP00000355069.4:p.Asp52=
ENST00000370296.6:c.159C>T ENSP00000359319.3:p.Asp53=
ENST00000427256.5:c.159C>T ENSP00000398652.1:p.Asp53=
ENST00000428433.5:c.159C>T ENSP00000396259.1:p.Asp53=
ENST00000483202.2:n.1161C>T
ENST00000553492.5:n.131+14128C>T
ENST00000554172.2:c.171C>T ENSP00000452489.2:p.Asp57=
ENST00000554363.2:n.125+3558C>T
NM_000278.3:c.159C>T NP_000269.2:p.Asp53=
NM_001304569.1:c.252C>T NP_001291498.1:p.Asp84=
NM_003987.3:c.159C>T NP_003978.2:p.Asp53=
NM_003988.3:c.159C>T NP_003979.2:p.Asp53=
NM_003989.3:c.159C>T NP_003980.2:p.Asp53=
NM_003990.3:c.159C>T NP_003981.2:p.Asp53=
NM_000278.4:c.159C>T NP_000269.3:p.Asp53=
NM_003987.4:c.159C>T NP_003978.3:p.Asp53=
NM_003988.4:c.159C>T NP_003979.2:p.Asp53=
NM_003989.4:c.159C>T NP_003980.3:p.Asp53=
NM_003990.4:c.159C>T NP_003981.3:p.Asp53=
NM_000278.5:c.159C>T MANE Select NP_000269.3:p.Asp53=
NM_001304569.2:c.252C>T NP_001291498.1:p.Asp84=
NM_003987.5:c.159C>T NP_003978.3:p.Asp53=
NM_003988.5:c.159C>T NP_003979.2:p.Asp53=
NM_003989.5:c.159C>T NP_003980.3:p.Asp53=
NM_003990.5:c.159C>T NP_003981.3:p.Asp53=