Canonical Allele Identifier: CA3733183

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32045345G>T , CM000668.2:g.32045345G>T	GRCh38
NC_000006.11:g.32013122G>T , CM000668.1:g.32013122G>T	GRCh37
NC_000006.10:g.32121100G>T	NCBI36
NG_008337.2:g.69030C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.10607-19C>A MANE Select	NP_001352205.1:n.10607-19C>A
ENST00000644971.2:c.10607-19C>A MANE Select	ENSP00000496448.1:n.10607-19C>A
NM_001365276.1:c.10607-19C>A	NP_001352205.1:n.10607-19C>A
NM_019105.6:c.10601-19C>A	NP_061978.6:n.10601-19C>A
NM_019105.7:c.10601-19C>A	NP_061978.6:n.10601-19C>A
NM_019105.8:c.10601-19C>A	NP_061978.6:n.10601-19C>A
NM_032470.3:c.-126C>A	NP_115859.2:n.-126C>A
NM_032470.4:c.-126C>A	NP_115859.2:n.-126C>A
ENST00000375244.7:c.10607-19C>A	ENSP00000364393.3:n.10607-19C>A
ENST00000451343.4:c.-126C>A	ENSP00000407685.1:n.-126C>A
ENST00000490077.5:n.434-19C>A
ENST00000611016.2:c.3761-19C>A	ENSP00000483409.1:n.3761-19C>A
ENST00000647633.1:c.11348-19C>A	ENSP00000497649.1:n.11348-19C>A