Canonical Allele Identifier: CA823930433

Gene: TNXB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32082981C>A , CM000668.2:g.32082981C>A	GRCh38
NC_000006.11:g.32050758C>A , CM000668.1:g.32050758C>A	GRCh37
NC_000006.10:g.32158736C>A	NCBI36
NG_008337.2:g.31394G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.3446-655G>T MANE Select	ENSP00000496448.1:n.3446-655G>T
ENST00000647633.1:c.4187-655G>T	ENSP00000497649.1:n.4187-655G>T
ENST00000375244.7:c.3446-655G>T	ENSP00000364393.3:n.3446-655G>T
ENST00000613214.4:c.3707-655G>T	ENSP00000480067.1:n.3707-655G>T
NM_019105.6:c.3446-655G>T	NP_061978.6:n.3446-655G>T
NM_001365276.1:c.3446-655G>T	NP_001352205.1:n.3446-655G>T
NM_019105.7:c.3446-655G>T	NP_061978.6:n.3446-655G>T
NM_001365276.2:c.3446-655G>T MANE Select	NP_001352205.1:n.3446-655G>T
NM_019105.8:c.3446-655G>T	NP_061978.6:n.3446-655G>T