Canonical Allele Identifier: CA2561439662
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595434dup , CM000681.2:g.3595434dup GRCh38
NC_000019.9:g.3595432dup , CM000681.1:g.3595432dup GRCh37
NC_000019.8:g.3546432dup NCBI36
NG_013363.1:g.16403dup , LRG_578:g.16403dup
NG_031943.1:g.14864dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*257dup MANE Select ENSP00000364336.4:n.*257dup
ENST00000375190.8:c.*257dup ENSP00000364336.3:n.*257dup
ENST00000411851.3:c.983+306dup ENSP00000393333.2:n.983+306dup
ENST00000589966.1:c.*120dup ENSP00000468145.1:n.*120dup
NM_001060.5:c.*257dup , LRG_578t1:c.*257dup NP_001051.1:n.*257dup
NM_201636.2:c.983+306dup NP_963998.2:n.983+306dup
NM_001060.6:c.*257dup MANE Select NP_001051.1:n.*257dup
NM_201636.3:c.983+306dup NP_963998.2:n.983+306dup