Canonical Allele Identifier: CA170656

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32048638G>A , CM000668.2:g.32048638G>A	GRCh38
NC_000006.11:g.32016415G>A , CM000668.1:g.32016415G>A	GRCh37
NC_000006.10:g.32124393G>A	NCBI36
NG_008337.2:g.65737C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.9770C>T MANE Select	NP_001352205.1:p.Thr3257Ile
ENST00000644971.2:c.9770C>T MANE Select	ENSP00000496448.1:p.Thr3257Ile
NM_001365276.1:c.9770C>T	NP_001352205.1:p.Thr3257Ile
NM_019105.6:c.9764C>T	NP_061978.6:p.Thr3255Ile
NM_019105.7:c.9764C>T	NP_061978.6:p.Thr3255Ile
NM_019105.8:c.9764C>T	NP_061978.6:p.Thr3255Ile
ENST00000375244.7:c.9770C>T	ENSP00000364393.3:p.Thr3257Ile
ENST00000611016.2:c.2924C>T	ENSP00000483409.1:p.Thr975Ile
ENST00000647633.1:c.10511C>T	ENSP00000497649.1:p.Thr3504Ile