Canonical Allele Identifier: CA881803980

Gene: TBXA2R

Linked Data

• dbSNP Id: rs1216308453
• MyVariant Identifiers: chr19:g.3595757_3595765del (hg19) ; chr19:g.3595759_3595767del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595761_3595769del , CM000681.2:g.3595761_3595769del	GRCh38
NC_000019.9:g.3595759_3595767del , CM000681.1:g.3595759_3595767del	GRCh37
NC_000019.8:g.3546759_3546767del	NCBI36
NG_013363.1:g.16067_16075del , LRG_578:g.16067_16075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.953_961del MANE Select	ENSP00000364336.4:p.Arg318_Gln320del
ENST00000375190.8:c.953_961del	ENSP00000364336.3:p.Arg318_Gln320del
ENST00000411851.3:c.953_961del	ENSP00000393333.2:p.Arg318_Gln320del
ENST00000589966.1:c.564_572del	ENSP00000468145.1:p.Ser189_Ala191del
NM_001060.5:c.953_961del , LRG_578t1:c.953_961del	NP_001051.1:p.Arg318_Gln320del
NM_201636.2:c.953_961del	NP_963998.2:p.Arg318_Gln320del
XM_011528214.1:c.953_961del	XP_011526516.1:p.Arg318_Gln320del
XM_011528214.2:c.953_961del	XP_011526516.1:p.Arg318_Gln320del
NM_001060.6:c.953_961del MANE Select	NP_001051.1:p.Arg318_Gln320del
NM_201636.3:c.953_961del	NP_963998.2:p.Arg318_Gln320del