Canonical Allele Identifier: CA3734579

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32068720A>G , CM000668.2:g.32068720A>G	GRCh38
NC_000006.11:g.32036497A>G , CM000668.1:g.32036497A>G	GRCh37
NC_000006.10:g.32144475A>G	NCBI36
NG_008337.2:g.45655T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.5903-13T>C MANE Select	NP_001352205.1:n.5903-13T>C
ENST00000644971.2:c.5903-13T>C MANE Select	ENSP00000496448.1:n.5903-13T>C
NM_001365276.1:c.5903-13T>C	NP_001352205.1:n.5903-13T>C
NM_019105.6:c.5903-13T>C	NP_061978.6:n.5903-13T>C
NM_019105.7:c.5903-13T>C	NP_061978.6:n.5903-13T>C
NM_019105.8:c.5903-13T>C	NP_061978.6:n.5903-13T>C
ENST00000375244.7:c.5903-13T>C	ENSP00000364393.3:n.5903-13T>C
ENST00000613214.4:c.6164-13T>C	ENSP00000480067.1:n.6164-13T>C
ENST00000647633.1:c.6644-13T>C	ENSP00000497649.1:n.6644-13T>C