Canonical Allele Identifier: CA3735211

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32084586G>T , CM000668.2:g.32084586G>T	GRCh38
NC_000006.11:g.32052363G>T , CM000668.1:g.32052363G>T	GRCh37
NC_000006.10:g.32160341G>T	NCBI36
NG_008337.2:g.29789C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.3272C>A MANE Select	NP_001352205.1:p.Ser1091Tyr
ENST00000644971.2:c.3272C>A MANE Select	ENSP00000496448.1:p.Ser1091Tyr
NM_001365276.1:c.3272C>A	NP_001352205.1:p.Ser1091Tyr
NM_019105.6:c.3272C>A	NP_061978.6:p.Ser1091Tyr
NM_019105.7:c.3272C>A	NP_061978.6:p.Ser1091Tyr
NM_019105.8:c.3272C>A	NP_061978.6:p.Ser1091Tyr
ENST00000375244.7:c.3272C>A	ENSP00000364393.3:p.Ser1091Tyr
ENST00000613214.4:c.3533C>A	ENSP00000480067.1:p.Ser1178Tyr
ENST00000647633.1:c.4013C>A	ENSP00000497649.1:p.Ser1338Tyr