Canonical Allele Identifier: CA920042082

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1568281532

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595408_3595417del , CM000681.2:g.3595408_3595417del	GRCh38
NC_000019.9:g.3595406_3595415del , CM000681.1:g.3595406_3595415del	GRCh37
NC_000019.8:g.3546406_3546415del	NCBI36
NG_013363.1:g.16420_16429del , LRG_578:g.16420_16429del
NG_031943.1:g.14838_14847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*274_*283del MANE Select	ENSP00000364336.4:n.*274_*283del
ENST00000375190.8:c.*274_*283del	ENSP00000364336.3:n.*274_*283del
ENST00000411851.3:c.983+323_984-329del	ENSP00000393333.2:n.983+323_984-329del
ENST00000589966.1:c.*137_*146del	ENSP00000468145.1:n.*137_*146del
NM_001060.5:c.*274_*283del , LRG_578t1:c.*274_*283del	NP_001051.1:n.*274_*283del
NM_201636.2:c.983+323_984-329del	NP_963998.2:n.983+323_984-329del
NM_001060.6:c.*274_*283del MANE Select	NP_001051.1:n.*274_*283del
NM_201636.3:c.983+323_984-329del	NP_963998.2:n.983+323_984-329del