Canonical Allele Identifier: CA1619427580

Gene: TNXB ATF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32108722G= , CM000668.2:g.32108722G=	GRCh38
NC_000006.11:g.32076499G= , CM000668.1:g.32076499G=	GRCh37
NC_000006.10:g.32184477G=	NCBI36
NG_008337.2:g.5653C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.-9+459C= (TNXB) MANE Select	NP_001352205.1:n.-9+459C=
ENST00000644971.2:c.-9+459C= (TNXB) MANE Select	ENSP00000496448.1:n.-9+459C=
NM_001365276.1:c.-9+459C= (TNXB)	NP_001352205.1:n.-9+459C=
NM_019105.6:c.-9+459C= (TNXB)	NP_061978.6:n.-9+459C=
NM_019105.7:c.-9+459C= (TNXB)	NP_061978.6:n.-9+459C=
NM_019105.8:c.-9+459C= (TNXB)	NP_061978.6:n.-9+459C=
ENST00000375244.7:c.-9+459C= (TNXB)	ENSP00000364393.3:n.-9+459C=
ENST00000442721.1:c.-9+6272C= (TNXB)	ENSP00000389946.1:n.-9+6272C=
ENST00000479795.1:c.-9+459C= (TNXB)	ENSP00000418248.1:n.-9+459C=
ENST00000486148.1:n.41+459C= (TNXB)
ENST00000494022.1:n.289+7982C= (ATF6B)
ENST00000647633.1:c.-9+459C= (TNXB)	ENSP00000497649.1:n.-9+459C=