Canonical Allele Identifier: CA1931936396
Gene: PAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100781320C= , CM000672.2:g.100781320C= GRCh38
NC_000010.10:g.102541077C= , CM000672.1:g.102541077C= GRCh37
NC_000010.9:g.102531067C= NCBI36
NG_008680.1:g.40610C=
NG_008680.2:g.50612C=

Transcript Alleles

HGVS Amino-acid change
ENST00000707078.1:c.664C= ENSP00000516729.1:p.Leu222=
ENST00000707079.1:c.571C= ENSP00000516730.1:p.Leu191=
ENST00000355243.8:c.571C= MANE Select ENSP00000347385.3:p.Leu191=
ENST00000427256.6:c.571C= ENSP00000398652.2:p.Leu191=
ENST00000679374.1:c.553C= ENSP00000506041.1:p.Leu185=
ENST00000355243.7:c.571C= ENSP00000347385.2:p.Leu191=
ENST00000361791.7:c.568C= ENSP00000355069.4:p.Leu190=
ENST00000370296.6:c.571C= ENSP00000359319.3:p.Leu191=
ENST00000427256.5:c.571C= ENSP00000398652.1:p.Leu191=
ENST00000428433.5:c.571C= ENSP00000396259.1:p.Leu191=
ENST00000553492.5:n.292C=
ENST00000554172.2:c.583C= ENSP00000452489.2:p.Leu195=
ENST00000554363.2:n.286C=
NM_000278.3:c.571C= NP_000269.2:p.Leu191=
NM_001304569.1:c.664C= NP_001291498.1:p.Leu222=
NM_003987.3:c.571C= NP_003978.2:p.Leu191=
NM_003988.3:c.571C= NP_003979.2:p.Leu191=
NM_003989.3:c.571C= NP_003980.2:p.Leu191=
NM_003990.3:c.571C= NP_003981.2:p.Leu191=
NM_000278.4:c.571C= NP_000269.3:p.Leu191=
NM_003987.4:c.571C= NP_003978.3:p.Leu191=
NM_003988.4:c.571C= NP_003979.2:p.Leu191=
NM_003989.4:c.571C= NP_003980.3:p.Leu191=
NM_003990.4:c.571C= NP_003981.3:p.Leu191=
NM_000278.5:c.571C= MANE Select NP_000269.3:p.Leu191=
NM_001304569.2:c.664C= NP_001291498.1:p.Leu222=
NM_003987.5:c.571C= NP_003978.3:p.Leu191=
NM_003988.5:c.571C= NP_003979.2:p.Leu191=
NM_003989.5:c.571C= NP_003980.3:p.Leu191=
NM_003990.5:c.571C= NP_003981.3:p.Leu191=