Canonical Allele Identifier: CA2584493795
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595598del , CM000681.2:g.3595598del GRCh38
NC_000019.9:g.3595596del , CM000681.1:g.3595596del GRCh37
NC_000019.8:g.3546596del NCBI36
NG_013363.1:g.16240del , LRG_578:g.16240del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*94del MANE Select ENSP00000364336.4:n.*94del
ENST00000375190.8:c.*94del ENSP00000364336.3:n.*94del
ENST00000411851.3:c.983+143del ENSP00000393333.2:n.983+143del
ENST00000589966.1:c.737del ENSP00000468145.1:p.Gly246ValfsTer27
NM_001060.5:c.*94del , LRG_578t1:c.*94del NP_001051.1:n.*94del
NM_201636.2:c.983+143del NP_963998.2:n.983+143del
XM_011528214.2:c.*94del XP_011526516.1:n.*94del
NM_001060.6:c.*94del MANE Select NP_001051.1:n.*94del
NM_201636.3:c.983+143del NP_963998.2:n.983+143del