Canonical Allele Identifier: CA920042087
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1599869252

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595785del , CM000681.2:g.3595785del GRCh38
NC_000019.9:g.3595783del , CM000681.1:g.3595783del GRCh37
NC_000019.8:g.3546783del NCBI36
NG_013363.1:g.16049del , LRG_578:g.16049del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.935del MANE Select ENSP00000364336.4:p.Arg312ProfsTer?
ENST00000375190.8:c.935del ENSP00000364336.3:p.Arg312ProfsTer?
ENST00000411851.3:c.935del ENSP00000393333.2:p.Arg312ProfsTer?
ENST00000589966.1:c.546del ENSP00000468145.1:p.Pro183ArgfsTer?
NM_001060.5:c.935del , LRG_578t1:c.935del NP_001051.1:p.Arg312ProfsTer?
NM_201636.2:c.935del NP_963998.2:p.Arg312ProfsTer?
XM_011528214.1:c.935del XP_011526516.1:p.Arg312ProfsTer?
XM_011528214.2:c.935del XP_011526516.1:p.Arg312ProfsTer?
NM_001060.6:c.935del MANE Select NP_001051.1:p.Arg312ProfsTer?
NM_201636.3:c.935del NP_963998.2:p.Arg312ProfsTer?