Canonical Allele Identifier: CA3733176

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32045256T>C , CM000668.2:g.32045256T>C	GRCh38
NC_000006.11:g.32013033T>C , CM000668.1:g.32013033T>C	GRCh37
NC_000006.10:g.32121011T>C	NCBI36
NG_008337.2:g.69119A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.10677A>G MANE Select	NP_001352205.1:p.Leu3559=
ENST00000644971.2:c.10677A>G MANE Select	ENSP00000496448.1:p.Leu3559=
NM_001365276.1:c.10677A>G	NP_001352205.1:p.Leu3559=
NM_019105.6:c.10671A>G	NP_061978.6:p.Leu3557=
NM_019105.7:c.10671A>G	NP_061978.6:p.Leu3557=
NM_019105.8:c.10671A>G	NP_061978.6:p.Leu3557=
NM_032470.3:c.-37A>G	NP_115859.2:n.-37A>G
NM_032470.4:c.-37A>G	NP_115859.2:n.-37A>G
ENST00000375244.7:c.10677A>G	ENSP00000364393.3:p.Leu3559=
ENST00000451343.4:c.-37A>G	ENSP00000407685.1:n.-37A>G
ENST00000490077.5:n.504A>G
ENST00000611016.2:c.3831A>G	ENSP00000483409.1:p.Leu1277=
ENST00000647633.1:c.11418A>G	ENSP00000497649.1:p.Leu3806=