Canonical Allele Identifier: CA2436171718

Gene: TEX11

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70605421C= , CM000685.2:g.70605421C=	GRCh38
NC_000023.10:g.69825271C= , CM000685.1:g.69825271C=	GRCh37
NC_000023.9:g.69741996C=	NCBI36
NG_012574.1:g.308297G=
NG_012574.2:g.308297G=

Transcript Alleles

HGVS	Amino-acid Change
NM_031276.3:c.2047G= MANE Select	NP_112566.2:p.Ala683=
ENST00000374333.7:c.2047G= MANE Select	ENSP00000363453.2:p.Ala683=
NM_001003811.1:c.2092G=	NP_001003811.1:p.Ala698=
NM_001003811.2:c.2092G=	NP_001003811.1:p.Ala698=
NM_031276.2:c.2047G=	NP_112566.2:p.Ala683=
ENST00000344304.3:c.2092G=	ENSP00000340995.3:p.Ala698=
ENST00000374320.6:c.1117G=	ENSP00000363440.2:p.Ala373=
ENST00000374333.6:c.2047G=	ENSP00000363453.2:p.Ala683=
ENST00000395889.6:c.2092G=	ENSP00000379226.2:p.Ala698=
XM_011530994.1:c.2047G=	XP_011529296.1:p.Ala683=
XM_011530995.1:c.1159G=	XP_011529297.1:p.Ala387=
XM_011530996.1:c.1117G=	XP_011529298.1:p.Ala373=
XM_017029649.1:c.2047G=	XP_016885138.1:p.Ala683=
XM_017029650.1:c.1159G=	XP_016885139.1:p.Ala387=
XM_017029651.1:c.1117G=	XP_016885140.1:p.Ala373=
XM_017029652.2:c.856G=	XP_016885141.1:p.Ala286=