Canonical Allele Identifier: CA2318945675

Gene: TBXA2R

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595479_3595481delinsAGG , CM000681.2:g.3595479_3595481delinsAGG	GRCh38
NC_000019.9:g.3595477_3595479delinsAGG , CM000681.1:g.3595477_3595479delinsAGG	GRCh37
NC_000019.8:g.3546477_3546479delinsAGG	NCBI36
NG_013363.1:g.16353_16355delinsCCT , LRG_578:g.16353_16355delinsCCT
NG_031943.1:g.14909_14911delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*207_*209delinsCCT MANE Select	ENSP00000364336.4:n.*207_*209delinsCCT
ENST00000375190.8:c.*207_*209delinsCCT	ENSP00000364336.3:n.*207_*209delinsCCT
ENST00000411851.3:c.983+256_983+258delinsCCT	ENSP00000393333.2:n.983+256_983+258delinsCCT
ENST00000589966.1:c.*70_*72delinsCCT	ENSP00000468145.1:n.*70_*72delinsCCT
NM_001060.5:c.*207_*209delinsCCT , LRG_578t1:c.*207_*209delinsCCT	NP_001051.1:n.*207_*209delinsCCT
NM_201636.2:c.983+256_983+258delinsCCT	NP_963998.2:n.983+256_983+258delinsCCT
NM_001060.6:c.*207_*209delinsCCT MANE Select	NP_001051.1:n.*207_*209delinsCCT
NM_201636.3:c.983+256_983+258delinsCCT	NP_963998.2:n.983+256_983+258delinsCCT