Canonical Allele Identifier: CA1619401122

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32042353G= , CM000668.2:g.32042353G=	GRCh38
NC_000006.11:g.32010130G= , CM000668.1:g.32010130G=	GRCh37
NC_000006.10:g.32118109G=	NCBI36
NG_007941.2:g.9046G=
NG_008337.2:g.72022C=
NG_007941.3:g.9049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.12220C= MANE Select	ENSP00000496448.1:p.Arg4074=
ENST00000647633.1:c.12961C=	ENSP00000497649.1:p.Arg4321=
ENST00000375244.7:c.12220C=	ENSP00000364393.3:p.Arg4074=
ENST00000451343.4:c.1507C=	ENSP00000407685.1:p.Arg503=
ENST00000490077.5:n.2047C=
ENST00000498094.1:n.705C=
ENST00000611016.2:c.5374C=	ENSP00000483409.1:p.Arg1792=
NM_019105.6:c.12214C=	NP_061978.6:p.Arg4072=
NM_032470.3:c.1507C=	NP_115859.2:p.Arg503=
NM_001365276.1:c.12220C=	NP_001352205.1:p.Arg4074=
NM_019105.7:c.12214C=	NP_061978.6:p.Arg4072=
NM_001365276.2:c.12220C= MANE Select	NP_001352205.1:p.Arg4074=
NM_019105.8:c.12214C=	NP_061978.6:p.Arg4072=
NM_032470.4:c.1507C=	NP_115859.2:p.Arg503=