Canonical Allele Identifier: CA2318945832

Gene: TBXA2R

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595758_3595767delinsGGCTGGAGAC , CM000681.2:g.3595758_3595767delinsGGCTGGAGAC	GRCh38
NC_000019.9:g.3595756_3595765delinsGGCTGGAGAC , CM000681.1:g.3595756_3595765delinsGGCTGGAGAC	GRCh37
NC_000019.8:g.3546756_3546765delinsGGCTGGAGAC	NCBI36
NG_013363.1:g.16067_16076delinsGTCTCCAGCC , LRG_578:g.16067_16076delinsGTCTCCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.953_962delinsGTCTCCAGCC MANE Select	ENSP00000364336.4:p.Arg318=
ENST00000375190.8:c.953_962delinsGTCTCCAGCC	ENSP00000364336.3:p.Arg318=
ENST00000411851.3:c.953_962delinsGTCTCCAGCC	ENSP00000393333.2:p.Arg318=
ENST00000589966.1:c.564_573delinsGTCTCCAGCC	ENSP00000468145.1:p.Ala188=
NM_001060.5:c.953_962delinsGTCTCCAGCC , LRG_578t1:c.953_962delinsGTCTCCAGCC	NP_001051.1:p.Arg318=
NM_201636.2:c.953_962delinsGTCTCCAGCC	NP_963998.2:p.Arg318=
XM_011528214.1:c.953_962delinsGTCTCCAGCC	XP_011526516.1:p.Arg318=
XM_011528214.2:c.953_962delinsGTCTCCAGCC	XP_011526516.1:p.Arg318=
NM_001060.6:c.953_962delinsGTCTCCAGCC MANE Select	NP_001051.1:p.Arg318=
NM_201636.3:c.953_962delinsGTCTCCAGCC	NP_963998.2:p.Arg318=