Canonical Allele Identifier: CA2318945826

Gene: TBXA2R

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595747_3595758delinsTGCTGAGGCGAG , CM000681.2:g.3595747_3595758delinsTGCTGAGGCGAG	GRCh38
NC_000019.9:g.3595745_3595756delinsTGCTGAGGCGAG , CM000681.1:g.3595745_3595756delinsTGCTGAGGCGAG	GRCh37
NC_000019.8:g.3546745_3546756delinsTGCTGAGGCGAG	NCBI36
NG_013363.1:g.16076_16087delinsCTCGCCTCAGCA , LRG_578:g.16076_16087delinsCTCGCCTCAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.962_973delinsCTCGCCTCAGCA MANE Select	ENSP00000364336.4:p.Pro321=
ENST00000375190.8:c.962_973delinsCTCGCCTCAGCA	ENSP00000364336.3:p.Pro321=
ENST00000411851.3:c.962_973delinsCTCGCCTCAGCA	ENSP00000393333.2:p.Pro321=
ENST00000589966.1:c.573_584delinsCTCGCCTCAGCA	ENSP00000468145.1:p.Ala191=
NM_001060.5:c.962_973delinsCTCGCCTCAGCA , LRG_578t1:c.962_973delinsCTCGCCTCAGCA	NP_001051.1:p.Pro321=
NM_201636.2:c.962_973delinsCTCGCCTCAGCA	NP_963998.2:p.Pro321=
XM_011528214.1:c.962_973delinsCTCGCCTCAGCA	XP_011526516.1:p.Pro321=
XM_011528214.2:c.962_973delinsCTCGCCTCAGCA	XP_011526516.1:p.Pro321=
NM_001060.6:c.962_973delinsCTCGCCTCAGCA MANE Select	NP_001051.1:p.Pro321=
NM_201636.3:c.962_973delinsCTCGCCTCAGCA	NP_963998.2:p.Pro321=