Canonical Allele Identifier: CA229729781

Gene: POU2F3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.120307511C>A , CM000673.2:g.120307511C>A	GRCh38
NC_000011.9:g.120178220C>A , CM000673.1:g.120178220C>A	GRCh37
NC_000011.8:g.119683430C>A	NCBI36
NG_030035.1:g.75872C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543440.7:c.802C>A MANE Select	ENSP00000441687.2:p.Pro268Thr
ENST00000260264.8:c.808C>A	ENSP00000260264.4:p.Pro270Thr
ENST00000532638.1:n.331C>A
ENST00000532663.1:c.175C>A	ENSP00000453150.2:p.Pro59Thr
ENST00000533620.5:c.*468C>A	ENSP00000435738.2:n.*468C>A
ENST00000543440.6:c.802C>A	ENSP00000441687.2:p.Pro268Thr
NM_001244682.1:c.808C>A	NP_001231611.1:p.Pro270Thr
NM_014352.3:c.802C>A	NP_055167.2:p.Pro268Thr
XM_011542739.1:c.790C>A	XP_011541041.1:p.Pro264Thr
XM_011542740.1:c.790C>A	XP_011541042.1:p.Pro264Thr
XM_011542741.1:c.703C>A	XP_011541043.1:p.Pro235Thr
XM_011542742.1:c.703C>A	XP_011541044.1:p.Pro235Thr
XM_011542743.1:c.703C>A	XP_011541045.1:p.Pro235Thr
XR_947818.1:n.952C>A
XM_011542739.2:c.790C>A	XP_011541041.1:p.Pro264Thr
XM_011542740.2:c.790C>A	XP_011541042.1:p.Pro264Thr
XM_011542741.3:c.703C>A	XP_011541043.1:p.Pro235Thr
XM_011542742.3:c.703C>A	XP_011541044.1:p.Pro235Thr
XM_011542743.2:c.703C>A	XP_011541045.1:p.Pro235Thr
XM_017017487.1:c.802C>A	XP_016872976.1:p.Pro268Thr
XM_024448424.1:c.766C>A	XP_024304192.1:p.Pro256Thr
NM_014352.4:c.802C>A MANE Select	NP_055167.2:p.Pro268Thr
NM_001244682.2:c.808C>A	NP_001231611.1:p.Pro270Thr