Canonical Allele Identifier: CA3733098

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32044582G>C , CM000668.2:g.32044582G>C	GRCh38
NC_000006.11:g.32012359G>C , CM000668.1:g.32012359G>C	GRCh37
NC_000006.10:g.32120338G>C	NCBI36
NG_008337.2:g.69793C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.11062C>G MANE Select	NP_001352205.1:p.Arg3688Gly
ENST00000644971.2:c.11062C>G MANE Select	ENSP00000496448.1:p.Arg3688Gly
NM_001365276.1:c.11062C>G	NP_001352205.1:p.Arg3688Gly
NM_019105.6:c.11056C>G	NP_061978.6:p.Arg3686Gly
NM_019105.7:c.11056C>G	NP_061978.6:p.Arg3686Gly
NM_019105.8:c.11056C>G	NP_061978.6:p.Arg3686Gly
NM_032470.3:c.349C>G	NP_115859.2:p.Arg117Gly
NM_032470.4:c.349C>G	NP_115859.2:p.Arg117Gly
ENST00000375244.7:c.11062C>G	ENSP00000364393.3:p.Arg3688Gly
ENST00000451343.4:c.349C>G	ENSP00000407685.1:p.Arg117Gly
ENST00000490077.5:n.889C>G
ENST00000611016.2:c.4216C>G	ENSP00000483409.1:p.Arg1406Gly
ENST00000647633.1:c.11803C>G	ENSP00000497649.1:p.Arg3935Gly