Canonical Allele Identifier: CA378257511

Gene: PAX2

Linked Data

• ClinVar Variation Id: 2110963
• ClinVar RCV Id: RCV003045779
• MyVariant Identifiers: chr10:g.102509551G>A (hg19) ; chr10:g.100749794G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100749794G>A , CM000672.2:g.100749794G>A	GRCh38
NC_000010.10:g.102509551G>A , CM000672.1:g.102509551G>A	GRCh37
NC_000010.9:g.102499541G>A	NCBI36
NG_008680.1:g.9084G>A
NG_008680.2:g.19086G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707078.1:c.185G>A	ENSP00000516729.1:p.Arg62Gln
ENST00000707079.1:c.92G>A	ENSP00000516730.1:p.Arg31Gln
ENST00000355243.8:c.92G>A MANE Select	ENSP00000347385.3:p.Arg31Gln
ENST00000427256.6:c.92G>A	ENSP00000398652.2:p.Arg31Gln
ENST00000679374.1:c.74G>A	ENSP00000506041.1:p.Arg25Gln
ENST00000355243.7:c.92G>A	ENSP00000347385.2:p.Arg31Gln
ENST00000361791.7:c.89G>A	ENSP00000355069.4:p.Arg30Gln
ENST00000370296.6:c.92G>A	ENSP00000359319.3:p.Arg31Gln
ENST00000427256.5:c.92G>A	ENSP00000398652.1:p.Arg31Gln
ENST00000428433.5:c.92G>A	ENSP00000396259.1:p.Arg31Gln
ENST00000483202.2:n.1094G>A
ENST00000553492.5:n.131+14061G>A
ENST00000554172.2:c.104G>A	ENSP00000452489.2:p.Arg35Gln
ENST00000554363.2:n.125+3491G>A
NM_000278.3:c.92G>A	NP_000269.2:p.Arg31Gln
NM_001304569.1:c.185G>A	NP_001291498.1:p.Arg62Gln
NM_003987.3:c.92G>A	NP_003978.2:p.Arg31Gln
NM_003988.3:c.92G>A	NP_003979.2:p.Arg31Gln
NM_003989.3:c.92G>A	NP_003980.2:p.Arg31Gln
NM_003990.3:c.92G>A	NP_003981.2:p.Arg31Gln
NM_000278.4:c.92G>A	NP_000269.3:p.Arg31Gln
NM_003987.4:c.92G>A	NP_003978.3:p.Arg31Gln
NM_003988.4:c.92G>A	NP_003979.2:p.Arg31Gln
NM_003989.4:c.92G>A	NP_003980.3:p.Arg31Gln
NM_003990.4:c.92G>A	NP_003981.3:p.Arg31Gln
NM_000278.5:c.92G>A MANE Select	NP_000269.3:p.Arg31Gln
NM_001304569.2:c.185G>A	NP_001291498.1:p.Arg62Gln
NM_003987.5:c.92G>A	NP_003978.3:p.Arg31Gln
NM_003988.5:c.92G>A	NP_003979.2:p.Arg31Gln
NM_003989.5:c.92G>A	NP_003980.3:p.Arg31Gln
NM_003990.5:c.92G>A	NP_003981.3:p.Arg31Gln