Canonical Allele Identifier: CA136898922

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32047651C>T , CM000668.2:g.32047651C>T	GRCh38
NC_000006.11:g.32015428C>T , CM000668.1:g.32015428C>T	GRCh37
NC_000006.10:g.32123406C>T	NCBI36
NG_008337.2:g.66724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.10324+83G>A MANE Select	ENSP00000496448.1:n.10324+83G>A
ENST00000647633.1:c.11065+83G>A	ENSP00000497649.1:n.11065+83G>A
ENST00000375244.7:c.10324+83G>A	ENSP00000364393.3:n.10324+83G>A
ENST00000611016.2:c.3478+83G>A	ENSP00000483409.1:n.3478+83G>A
NM_019105.6:c.10318+83G>A	NP_061978.6:n.10318+83G>A
NM_001365276.1:c.10324+83G>A	NP_001352205.1:n.10324+83G>A
NM_019105.7:c.10318+83G>A	NP_061978.6:n.10318+83G>A
NM_001365276.2:c.10324+83G>A MANE Select	NP_001352205.1:n.10324+83G>A
NM_019105.8:c.10318+83G>A	NP_061978.6:n.10318+83G>A