Canonical Allele Identifier: CA2318945802

Gene: TBXA2R

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595709_3595710delinsCG , CM000681.2:g.3595709_3595710delinsCG	GRCh38
NC_000019.9:g.3595707_3595708delinsCG , CM000681.1:g.3595707_3595708delinsCG	GRCh37
NC_000019.8:g.3546707_3546708delinsCG	NCBI36
NG_013363.1:g.16124_16125delinsCG , LRG_578:g.16124_16125delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.1010_1011delinsCG MANE Select	ENSP00000364336.4:p.Thr337=
ENST00000375190.8:c.1010_1011delinsCG	ENSP00000364336.3:p.Thr337=
ENST00000411851.3:c.983+27_983+28delinsCG	ENSP00000393333.2:n.983+27_983+28delinsCG
ENST00000589966.1:c.621_622delinsCG	ENSP00000468145.1:p.His207=
NM_001060.5:c.1010_1011delinsCG , LRG_578t1:c.1010_1011delinsCG	NP_001051.1:p.Thr337=
NM_201636.2:c.983+27_983+28delinsCG	NP_963998.2:n.983+27_983+28delinsCG
XM_011528214.1:c.1010_1011delinsCG	XP_011526516.1:p.Thr337=
XM_011528214.2:c.1010_1011delinsCG	XP_011526516.1:p.Thr337=
NM_001060.6:c.1010_1011delinsCG MANE Select	NP_001051.1:p.Thr337=
NM_201636.3:c.983+27_983+28delinsCG	NP_963998.2:n.983+27_983+28delinsCG