Canonical Allele Identifier: CA3732900

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32042684C>T , CM000668.2:g.32042684C>T	GRCh38
NC_000006.11:g.32010461C>T , CM000668.1:g.32010461C>T	GRCh37
NC_000006.10:g.32118440C>T	NCBI36
NG_007941.2:g.9377C>T
NG_008337.2:g.71691G>A
NG_007941.3:g.9380C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.12058+15G>A MANE Select	ENSP00000496448.1:n.12058+15G>A
ENST00000647633.1:c.12799+15G>A	ENSP00000497649.1:n.12799+15G>A
ENST00000375244.7:c.12058+15G>A	ENSP00000364393.3:n.12058+15G>A
ENST00000451343.4:c.1345+15G>A	ENSP00000407685.1:n.1345+15G>A
ENST00000490077.5:n.1885+15G>A
ENST00000498094.1:n.543+15G>A
ENST00000611016.2:c.5212+15G>A	ENSP00000483409.1:n.5212+15G>A
NM_019105.6:c.12052+15G>A	NP_061978.6:n.12052+15G>A
NM_032470.3:c.1345+15G>A	NP_115859.2:n.1345+15G>A
NM_001365276.1:c.12058+15G>A	NP_001352205.1:n.12058+15G>A
NM_019105.7:c.12052+15G>A	NP_061978.6:n.12052+15G>A
NM_001365276.2:c.12058+15G>A MANE Select	NP_001352205.1:n.12058+15G>A
NM_019105.8:c.12052+15G>A	NP_061978.6:n.12052+15G>A
NM_032470.4:c.1345+15G>A	NP_115859.2:n.1345+15G>A