Canonical Allele Identifier: CA1619401604

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32042955T= , CM000668.2:g.32042955T=	GRCh38
NC_000006.11:g.32010732T= , CM000668.1:g.32010732T=	GRCh37
NC_000006.10:g.32118711T=	NCBI36
NG_007941.2:g.9648T=
NG_008337.2:g.71420A=
NG_007941.3:g.9651T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.11921A= MANE Select	ENSP00000496448.1:p.Asn3974=
ENST00000647633.1:c.12662A=	ENSP00000497649.1:p.Asn4221=
ENST00000375244.7:c.11921A=	ENSP00000364393.3:p.Asn3974=
ENST00000451343.4:c.1208A=	ENSP00000407685.1:p.Asn403=
ENST00000490077.5:n.1748A=
ENST00000498094.1:n.287A=
ENST00000611016.2:c.5075A=	ENSP00000483409.1:p.Asn1692=
NM_019105.6:c.11915A=	NP_061978.6:p.Asn3972=
NM_032470.3:c.1208A=	NP_115859.2:p.Asn403=
NM_001365276.1:c.11921A=	NP_001352205.1:p.Asn3974=
NM_019105.7:c.11915A=	NP_061978.6:p.Asn3972=
NM_001365276.2:c.11921A= MANE Select	NP_001352205.1:p.Asn3974=
NM_019105.8:c.11915A=	NP_061978.6:p.Asn3972=
NM_032470.4:c.1208A=	NP_115859.2:p.Asn403=