Canonical Allele Identifier: CA3733669

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32052735T>C , CM000668.2:g.32052735T>C	GRCh38
NC_000006.11:g.32020512T>C , CM000668.1:g.32020512T>C	GRCh37
NC_000006.10:g.32128490T>C	NCBI36
NG_008337.2:g.61640A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.9050A>G MANE Select	NP_001352205.1:p.Lys3017Arg
ENST00000644971.2:c.9050A>G MANE Select	ENSP00000496448.1:p.Lys3017Arg
NM_001365276.1:c.9050A>G	NP_001352205.1:p.Lys3017Arg
NM_019105.6:c.9044A>G	NP_061978.6:p.Lys3015Arg
NM_019105.7:c.9044A>G	NP_061978.6:p.Lys3015Arg
NM_019105.8:c.9044A>G	NP_061978.6:p.Lys3015Arg
ENST00000375244.7:c.9050A>G	ENSP00000364393.3:p.Lys3017Arg
ENST00000611016.2:c.2204A>G	ENSP00000483409.1:p.Lys735Arg
ENST00000647633.1:c.9791A>G	ENSP00000497649.1:p.Lys3264Arg