Canonical Allele Identifier: CA2842946513

Gene: PAX8 PAX8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113244415T>C , CM000664.2:g.113244415T>C	GRCh38
NC_000002.11:g.114001992T>C , CM000664.1:g.114001992T>C	GRCh37
NC_000002.10:g.113718462T>C	NCBI36
NG_012384.1:g.39507A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468980.4:c.389+12A>G (PAX8)	ENSP00000451240.2:n.389+12A>G
ENST00000429538.8:c.389+12A>G (PAX8) MANE Select	ENSP00000395498.3:n.389+12A>G
ENST00000681162.1:c.389+12A>G (PAX8)	ENSP00000505425.1:n.389+12A>G
ENST00000263334.9:c.389+12A>G (PAX8)	ENSP00000263334.6:n.389+12A>G
ENST00000263335.11:c.389+12A>G (PAX8)	ENSP00000263335.7:n.389+12A>G
ENST00000348715.9:c.389+12A>G (PAX8)	ENSP00000314750.5:n.389+12A>G
ENST00000397647.7:c.389+12A>G (PAX8)	ENSP00000380768.3:n.389+12A>G
ENST00000429538.7:c.389+12A>G (PAX8)	ENSP00000395498.3:n.389+12A>G
ENST00000467778.5:n.553+12A>G (PAX8)
ENST00000554830.2:c.-40-1637A>G (PAX8)	ENSP00000451213.2:n.-40-1637A>G
NM_003466.3:c.389+12A>G (PAX8)	NP_003457.1:n.389+12A>G
NM_013952.3:c.389+12A>G (PAX8)	NP_039246.1:n.389+12A>G
NM_013953.3:c.389+12A>G (PAX8)	NP_039247.1:n.389+12A>G
NM_013992.3:c.389+12A>G (PAX8)	NP_054698.1:n.389+12A>G
NR_015377.2:n.355-6352T>C (PAX8-AS1)
XM_011511790.1:c.560+12A>G (PAX8)	XP_011510092.1:n.560+12A>G
XM_011511791.1:c.560+12A>G (PAX8)	XP_011510093.1:n.560+12A>G
XM_011511792.1:c.560+12A>G (PAX8)	XP_011510094.1:n.560+12A>G
XM_011511793.1:c.560+12A>G (PAX8)	XP_011510095.1:n.560+12A>G
XM_011511794.1:c.389+12A>G (PAX8)	XP_011510096.1:n.389+12A>G
XR_923021.1:n.587+12A>G (PAX8)
NM_003466.4:c.389+12A>G (PAX8) MANE Select	NP_003457.1:n.389+12A>G
NM_013952.4:c.389+12A>G (PAX8)	NP_039246.1:n.389+12A>G
NM_013953.4:c.389+12A>G (PAX8)	NP_039247.1:n.389+12A>G
NM_013992.4:c.389+12A>G (PAX8)	NP_054698.1:n.389+12A>G