Canonical Allele Identifier: CA2584493822
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595838dup , CM000681.2:g.3595838dup GRCh38
NC_000019.9:g.3595836dup , CM000681.1:g.3595836dup GRCh37
NC_000019.8:g.3546836dup NCBI36
NG_013363.1:g.15996dup , LRG_578:g.15996dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.882dup MANE Select ENSP00000364336.4:p.Arg295AlafsTer?
ENST00000375190.8:c.882dup ENSP00000364336.3:p.Arg295AlafsTer?
ENST00000411851.3:c.882dup ENSP00000393333.2:p.Arg295AlafsTer?
ENST00000589966.1:c.493dup ENSP00000468145.1:p.Ala165GlyfsTer?
NM_001060.5:c.882dup , LRG_578t1:c.882dup NP_001051.1:p.Arg295AlafsTer?
NM_201636.2:c.882dup NP_963998.2:p.Arg295AlafsTer?
XM_011528214.1:c.882dup XP_011526516.1:p.Arg295AlafsTer?
XM_011528214.2:c.882dup XP_011526516.1:p.Arg295AlafsTer?
NM_001060.6:c.882dup MANE Select NP_001051.1:p.Arg295AlafsTer?
NM_201636.3:c.882dup NP_963998.2:p.Arg295AlafsTer?