Canonical Allele Identifier: CA2544110022
Gene: PAX8 HGNC NCBI
PAX8-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113246590_113246591insCCGAATGGAATGGAATGCAATGGAATG , CM000664.2:g.113246590_113246591insCCGAATGGAATGGAATGCAATGGAATG GRCh38
NC_000002.11:g.114004167_114004168insCCGAATGGAATGGAATGCAATGGAATG , CM000664.1:g.114004167_114004168insCCGAATGGAATGGAATGCAATGGAATG GRCh37
NC_000002.10:g.113720637_113720638insCCGAATGGAATGGAATGCAATGGAATG NCBI36
NG_012384.1:g.37331_37332insCATTCCATTGCATTCCATTCCATTCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000468980.4:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000451240.2:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000429538.8:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) MANE Select ENSP00000395498.3:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000681162.1:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000505425.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000263334.9:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000263334.6:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000263335.11:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000263335.7:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000348715.9:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000314750.5:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000397647.7:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000380768.3:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000429538.7:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000395498.3:n.191+163_191+164insCATTCCATTGCATTCCATTCCAT...
ENST00000467778.5:n.355+163_355+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8)
ENST00000554830.2:c.-40-3813_-40-3812insCATTCCATTGCATTCCATTCCATTCGG (PAX8) ENSP00000451213.2:n.-40-3813_-40-3812insCATTCCATTGCATTCCATTCC...
NM_003466.3:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_003457.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013952.3:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_039246.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013953.3:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_039247.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013992.3:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_054698.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NR_015377.2:n.355-4177_355-4176insCCGAATGGAATGGAATGCAATGGAATG (PAX8-AS1)
XM_011511790.1:c.359+163_359+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) XP_011510092.1:n.359+163_359+164insCATTCCATTGCATTCCATTCCATTCG...
XM_011511791.1:c.359+163_359+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) XP_011510093.1:n.359+163_359+164insCATTCCATTGCATTCCATTCCATTCG...
XM_011511792.1:c.359+163_359+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) XP_011510094.1:n.359+163_359+164insCATTCCATTGCATTCCATTCCATTCG...
XM_011511793.1:c.359+163_359+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) XP_011510095.1:n.359+163_359+164insCATTCCATTGCATTCCATTCCATTCG...
XM_011511794.1:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) XP_011510096.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCG...
XR_923021.1:n.386+163_386+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8)
NM_003466.4:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) MANE Select NP_003457.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013952.4:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_039246.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013953.4:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_039247.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG
NM_013992.4:c.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG (PAX8) NP_054698.1:n.191+163_191+164insCATTCCATTGCATTCCATTCCATTCGG