Canonical Allele Identifier: CA363549953

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32056702C>T , CM000668.2:g.32056702C>T	GRCh38
NC_000006.11:g.32024479C>T , CM000668.1:g.32024479C>T	GRCh37
NC_000006.10:g.32132457C>T	NCBI36
NG_008337.2:g.57673G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.8027G>A MANE Select	NP_001352205.1:p.Gly2676Glu
ENST00000644971.2:c.8027G>A MANE Select	ENSP00000496448.1:p.Gly2676Glu
NM_001365276.1:c.8027G>A	NP_001352205.1:p.Gly2676Glu
NM_019105.6:c.8027G>A	NP_061978.6:p.Gly2676Glu
NM_019105.7:c.8027G>A	NP_061978.6:p.Gly2676Glu
NM_019105.8:c.8027G>A	NP_061978.6:p.Gly2676Glu
ENST00000375244.7:c.8027G>A	ENSP00000364393.3:p.Gly2676Glu
ENST00000611016.2:c.1187G>A	ENSP00000483409.1:p.Gly396Glu
ENST00000647633.1:c.8768G>A	ENSP00000497649.1:p.Gly2923Glu