Canonical Allele Identifier: CA3733177

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32045260C>T , CM000668.2:g.32045260C>T	GRCh38
NC_000006.11:g.32013037C>T , CM000668.1:g.32013037C>T	GRCh37
NC_000006.10:g.32121015C>T	NCBI36
NG_008337.2:g.69115G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.10673G>A MANE Select	NP_001352205.1:p.Arg3558His
ENST00000644971.2:c.10673G>A MANE Select	ENSP00000496448.1:p.Arg3558His
NM_001365276.1:c.10673G>A	NP_001352205.1:p.Arg3558His
NM_019105.6:c.10667G>A	NP_061978.6:p.Arg3556His
NM_019105.7:c.10667G>A	NP_061978.6:p.Arg3556His
NM_019105.8:c.10667G>A	NP_061978.6:p.Arg3556His
NM_032470.3:c.-41G>A	NP_115859.2:n.-41G>A
NM_032470.4:c.-41G>A	NP_115859.2:n.-41G>A
ENST00000375244.7:c.10673G>A	ENSP00000364393.3:p.Arg3558His
ENST00000451343.4:c.-41G>A	ENSP00000407685.1:n.-41G>A
ENST00000490077.5:n.500G>A
ENST00000611016.2:c.3827G>A	ENSP00000483409.1:p.Arg1276His
ENST00000647633.1:c.11414G>A	ENSP00000497649.1:p.Arg3805His