Canonical Allele Identifier: CA3732831

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32042416dup , CM000668.2:g.32042416dup	GRCh38
NC_000006.11:g.32010193dup , CM000668.1:g.32010193dup	GRCh37
NC_000006.10:g.32118172dup	NCBI36
NG_007941.2:g.9109dup
NG_008337.2:g.71959dup
NG_007941.3:g.9112dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.12210+39dup MANE Select	ENSP00000496448.1:n.12210+39dup
ENST00000647633.1:c.12951+39dup	ENSP00000497649.1:n.12951+39dup
ENST00000375244.7:c.12210+39dup	ENSP00000364393.3:n.12210+39dup
ENST00000451343.4:c.1497+39dup	ENSP00000407685.1:n.1497+39dup
ENST00000490077.5:n.2037+39dup
ENST00000498094.1:n.695+39dup
ENST00000611016.2:c.5364+39dup	ENSP00000483409.1:n.5364+39dup
NM_019105.6:c.12204+39dup	NP_061978.6:n.12204+39dup
NM_032470.3:c.1497+39dup	NP_115859.2:n.1497+39dup
NM_001365276.1:c.12210+39dup	NP_001352205.1:n.12210+39dup
NM_019105.7:c.12204+39dup	NP_061978.6:n.12204+39dup
NM_001365276.2:c.12210+39dup MANE Select	NP_001352205.1:n.12210+39dup
NM_019105.8:c.12204+39dup	NP_061978.6:n.12204+39dup
NM_032470.4:c.1497+39dup	NP_115859.2:n.1497+39dup