Canonical Allele Identifier: CA136902498

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32052461A>G , CM000668.2:g.32052461A>G	GRCh38
NC_000006.11:g.32020238A>G , CM000668.1:g.32020238A>G	GRCh37
NC_000006.10:g.32128216A>G	NCBI36
NG_008337.2:g.61914T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.9115+209T>C MANE Select	NP_001352205.1:n.9115+209T>C
ENST00000644971.2:c.9115+209T>C MANE Select	ENSP00000496448.1:n.9115+209T>C
NM_001365276.1:c.9115+209T>C	NP_001352205.1:n.9115+209T>C
NM_019105.6:c.9109+209T>C	NP_061978.6:n.9109+209T>C
NM_019105.7:c.9109+209T>C	NP_061978.6:n.9109+209T>C
NM_019105.8:c.9109+209T>C	NP_061978.6:n.9109+209T>C
ENST00000375244.7:c.9115+209T>C	ENSP00000364393.3:n.9115+209T>C
ENST00000611016.2:c.2269+209T>C	ENSP00000483409.1:n.2269+209T>C
ENST00000647633.1:c.9856+209T>C	ENSP00000497649.1:n.9856+209T>C