Canonical Allele Identifier: CA348302717

Gene: PAX8 PAX8-AS1

Linked Data

• ClinVar Variation Id: 915464
• ClinVar RCV Id: RCV001170073
• dbSNP Id: rs1691154033
• MyVariant Identifiers: chr2:g.114002157G>A (hg19) ; chr2:g.113244580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113244580G>A , CM000664.2:g.113244580G>A	GRCh38
NC_000002.11:g.114002157G>A , CM000664.1:g.114002157G>A	GRCh37
NC_000002.10:g.113718627G>A	NCBI36
NG_012384.1:g.39342C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468980.4:c.236C>T (PAX8)	ENSP00000451240.2:p.Ser79Phe
ENST00000429538.8:c.236C>T (PAX8) MANE Select	ENSP00000395498.3:p.Ser79Phe
ENST00000681162.1:c.236C>T (PAX8)	ENSP00000505425.1:p.Ser79Phe
ENST00000263334.9:c.236C>T (PAX8)	ENSP00000263334.6:p.Ser79Phe
ENST00000263335.11:c.236C>T (PAX8)	ENSP00000263335.7:p.Ser79Phe
ENST00000348715.9:c.236C>T (PAX8)	ENSP00000314750.5:p.Ser79Phe
ENST00000397647.7:c.236C>T (PAX8)	ENSP00000380768.3:p.Ser79Phe
ENST00000429538.7:c.236C>T (PAX8)	ENSP00000395498.3:p.Ser79Phe
ENST00000467778.5:n.400C>T (PAX8)
ENST00000554830.2:c.-40-1802C>T (PAX8)	ENSP00000451213.2:n.-40-1802C>T
NM_003466.3:c.236C>T (PAX8)	NP_003457.1:p.Ser79Phe
NM_013952.3:c.236C>T (PAX8)	NP_039246.1:p.Ser79Phe
NM_013953.3:c.236C>T (PAX8)	NP_039247.1:p.Ser79Phe
NM_013992.3:c.236C>T (PAX8)	NP_054698.1:p.Ser79Phe
NR_015377.2:n.355-6187G>A (PAX8-AS1)
XM_011511790.1:c.407C>T (PAX8)	XP_011510092.1:p.Ser136Phe
XM_011511791.1:c.407C>T (PAX8)	XP_011510093.1:p.Ser136Phe
XM_011511792.1:c.407C>T (PAX8)	XP_011510094.1:p.Ser136Phe
XM_011511793.1:c.407C>T (PAX8)	XP_011510095.1:p.Ser136Phe
XM_011511794.1:c.236C>T (PAX8)	XP_011510096.1:p.Ser79Phe
XR_923021.1:n.434C>T (PAX8)
NM_003466.4:c.236C>T (PAX8) MANE Select	NP_003457.1:p.Ser79Phe
NM_013952.4:c.236C>T (PAX8)	NP_039246.1:p.Ser79Phe
NM_013953.4:c.236C>T (PAX8)	NP_039247.1:p.Ser79Phe
NM_013992.4:c.236C>T (PAX8)	NP_054698.1:p.Ser79Phe