Canonical Allele Identifier: CA3733527

Gene: TNXB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32049635C>A , CM000668.2:g.32049635C>A	GRCh38
NC_000006.11:g.32017412C>A , CM000668.1:g.32017412C>A	GRCh37
NC_000006.10:g.32125390C>A	NCBI36
NG_008337.2:g.64740G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001365276.2:c.9440-48G>T MANE Select	NP_001352205.1:n.9440-48G>T
ENST00000644971.2:c.9440-48G>T MANE Select	ENSP00000496448.1:n.9440-48G>T
NM_001365276.1:c.9440-48G>T	NP_001352205.1:n.9440-48G>T
NM_019105.6:c.9434-48G>T	NP_061978.6:n.9434-48G>T
NM_019105.7:c.9434-48G>T	NP_061978.6:n.9434-48G>T
NM_019105.8:c.9434-48G>T	NP_061978.6:n.9434-48G>T
ENST00000375244.7:c.9440-48G>T	ENSP00000364393.3:n.9440-48G>T
ENST00000611016.2:c.2594-48G>T	ENSP00000483409.1:n.2594-48G>T
ENST00000647633.1:c.10181-48G>T	ENSP00000497649.1:n.10181-48G>T