Canonical Allele Identifier: CA2584493774
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595532-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595536del , CM000681.2:g.3595536del GRCh38
NC_000019.9:g.3595534del , CM000681.1:g.3595534del GRCh37
NC_000019.8:g.3546534del NCBI36
NG_013363.1:g.16301del , LRG_578:g.16301del
NG_031943.1:g.14966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*155del MANE Select ENSP00000364336.4:n.*155del
ENST00000375190.8:c.*155del ENSP00000364336.3:n.*155del
ENST00000411851.3:c.983+204del ENSP00000393333.2:n.983+204del
ENST00000589966.1:c.*18del ENSP00000468145.1:n.*18del
NM_001060.5:c.*155del , LRG_578t1:c.*155del NP_001051.1:n.*155del
NM_201636.2:c.983+204del NP_963998.2:n.983+204del
NM_001060.6:c.*155del MANE Select NP_001051.1:n.*155del
NM_201636.3:c.983+204del NP_963998.2:n.983+204del
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