Canonical Allele Identifier: CA2584493814
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595682del , CM000681.2:g.3595682del GRCh38
NC_000019.9:g.3595680del , CM000681.1:g.3595680del GRCh37
NC_000019.8:g.3546680del NCBI36
NG_013363.1:g.16153del , LRG_578:g.16153del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*7del MANE Select ENSP00000364336.4:n.*7del
ENST00000375190.8:c.*7del ENSP00000364336.3:n.*7del
ENST00000411851.3:c.983+56del ENSP00000393333.2:n.983+56del
ENST00000589966.1:c.650del ENSP00000468145.1:p.Gly217AspfsTer?
NM_001060.5:c.*7del , LRG_578t1:c.*7del NP_001051.1:n.*7del
NM_201636.2:c.983+56del NP_963998.2:n.983+56del
XM_011528214.1:c.*7del XP_011526516.1:n.*7del
XM_011528214.2:c.*7del XP_011526516.1:n.*7del
NM_001060.6:c.*7del MANE Select NP_001051.1:n.*7del
NM_201636.3:c.983+56del NP_963998.2:n.983+56del