Canonical Allele Identifier: CA3733038

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32043937A>G , CM000668.2:g.32043937A>G	GRCh38
NC_000006.11:g.32011714A>G , CM000668.1:g.32011714A>G	GRCh37
NC_000006.10:g.32119693A>G	NCBI36
NG_008337.2:g.70438T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.11387-45T>C MANE Select	NP_001352205.1:n.11387-45T>C
ENST00000644971.2:c.11387-45T>C MANE Select	ENSP00000496448.1:n.11387-45T>C
NM_001365276.1:c.11387-45T>C	NP_001352205.1:n.11387-45T>C
NM_019105.6:c.11381-45T>C	NP_061978.6:n.11381-45T>C
NM_019105.7:c.11381-45T>C	NP_061978.6:n.11381-45T>C
NM_019105.8:c.11381-45T>C	NP_061978.6:n.11381-45T>C
NM_032470.3:c.674-45T>C	NP_115859.2:n.674-45T>C
NM_032470.4:c.674-45T>C	NP_115859.2:n.674-45T>C
ENST00000375244.7:c.11387-45T>C	ENSP00000364393.3:n.11387-45T>C
ENST00000451343.4:c.674-45T>C	ENSP00000407685.1:n.674-45T>C
ENST00000490077.5:n.1214-45T>C
ENST00000611016.2:c.4541-45T>C	ENSP00000483409.1:n.4541-45T>C
ENST00000647633.1:c.12128-45T>C	ENSP00000497649.1:n.12128-45T>C