Canonical Allele Identifier: CA992743547
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595387_3595388del , CM000681.2:g.3595387_3595388del GRCh38
NC_000019.9:g.3595385_3595386del , CM000681.1:g.3595385_3595386del GRCh37
NC_000019.8:g.3546385_3546386del NCBI36
NG_013363.1:g.16455_16456del , LRG_578:g.16455_16456del
NG_031943.1:g.14817_14818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*309_*310del MANE Select ENSP00000364336.4:n.*309_*310del
ENST00000375190.8:c.*309_*310del ENSP00000364336.3:n.*309_*310del
ENST00000411851.3:c.984-303_984-302del ENSP00000393333.2:n.984-303_984-302del
ENST00000589966.1:c.*172_*173del ENSP00000468145.1:n.*172_*173del
NM_001060.5:c.*309_*310del , LRG_578t1:c.*309_*310del NP_001051.1:n.*309_*310del
NM_201636.2:c.984-303_984-302del NP_963998.2:n.984-303_984-302del
NM_001060.6:c.*309_*310del MANE Select NP_001051.1:n.*309_*310del
NM_201636.3:c.984-303_984-302del NP_963998.2:n.984-303_984-302del