Canonical Allele Identifier: CA1701385135

Gene: POU6F2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39197987T= , CM000669.2:g.39197987T=	GRCh38
NC_000007.13:g.39237586T= , CM000669.1:g.39237586T=	GRCh37
NC_000007.12:g.39204111T=	NCBI36
NG_016022.1:g.224978T=
NG_016022.2:g.225110T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403058.6:c.191-6248T=	ENSP00000384004.1:n.191-6248T=
ENST00000518318.7:c.278-6248T= MANE Select	ENSP00000430514.3:n.278-6248T=
ENST00000673818.5:n.268-6248T=
ENST00000673891.1:c.*278-6248T=	ENSP00000501205.1:n.*278-6248T=
ENST00000674059.1:c.*278-6248T=	ENSP00000500997.1:n.*278-6248T=
ENST00000403058.5:c.191-6248T=	ENSP00000384004.1:n.191-6248T=
ENST00000451021.5:c.194-6248T=	ENSP00000409684.1:n.194-6248T=
ENST00000517348.1:n.652-6248T=
ENST00000518318.6:c.191-6248T=	ENSP00000430514.2:n.191-6248T=
ENST00000520104.5:c.167-6248T=	ENSP00000453020.1:n.167-6248T=
ENST00000524147.5:c.167-6248T=	ENSP00000452911.1:n.167-6248T=
ENST00000559001.5:c.167-6248T=	ENSP00000452633.1:n.167-6248T=
NM_001166018.1:c.191-6248T=	NP_001159490.1:n.191-6248T=
NM_007252.3:c.191-6248T=	NP_009183.3:n.191-6248T=
XM_011515113.1:c.278-6248T=	XP_011513415.1:n.278-6248T=
XM_011515113.2:c.278-6248T=	XP_011513415.1:n.278-6248T=
NM_001166018.2:c.191-6248T=	NP_001159490.1:n.191-6248T=
NM_001370959.1:c.278-6248T= MANE Select	NP_001357888.1:n.278-6248T=
NM_007252.4:c.191-6248T=	NP_009183.3:n.191-6248T=