Canonical Allele Identifier: CA2573054519

Gene: TBX4

Linked Data

• ClinVar Variation Id: 1341416
• ClinVar RCV Id: RCV001829330
• dbSNP Id: rs2143792602

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61456640del , CM000679.2:g.61456640del	GRCh38
NC_000017.10:g.59534001del , CM000679.1:g.59534001del	GRCh37
NC_000017.9:g.56888783del	NCBI36
NG_008080.1:g.5195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642491.1:c.150del	ENSP00000495714.1:p.Ala52ProfsTer?
ENST00000644296.1:c.150del MANE Select	ENSP00000495986.1:p.Ala52ProfsTer?
ENST00000240335.1:c.150del	ENSP00000240335.1:p.Ala52ProfsTer?
ENST00000393853.8:c.150del	ENSP00000377435.3:p.Ala52ProfsTer?
ENST00000589003.5:c.-109del	ENSP00000467588.1:n.-109del
NM_018488.2:c.150del	NP_060958.2:p.Ala52ProfsTer?
XM_005257835.3:c.150del	XP_005257892.2:p.Ala52ProfsTer?
XM_005257837.2:c.150del	XP_005257894.1:p.Ala52ProfsTer?
XM_011525490.1:c.339del	XP_011523792.1:p.Ala115ProfsTer?
XM_011525491.1:c.339del	XP_011523793.1:p.Ala115ProfsTer?
XM_011525492.1:c.150del	XP_011523794.1:p.Ala52ProfsTer?
XM_011525493.1:c.150del	XP_011523795.1:p.Ala52ProfsTer?
XM_011525494.1:c.150del	XP_011523796.1:p.Ala52ProfsTer?
XM_011525495.1:c.339del	XP_011523797.1:p.Ala115ProfsTer?
NM_001321120.2:c.150del MANE Select	NP_001308049.1:p.Ala52ProfsTer?
NM_018488.3:c.150del	NP_060958.2:p.Ala52ProfsTer?
XM_011525490.2:c.339del	XP_011523792.1:p.Ala115ProfsTer?
XM_011525491.2:c.339del	XP_011523793.1:p.Ala115ProfsTer?
XM_011525495.2:c.339del	XP_011523797.1:p.Ala115ProfsTer?