Canonical Allele Identifier: CA2269031002

Gene: TBX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61455987_61455989delinsCCT , CM000679.2:g.61455987_61455989delinsCCT	GRCh38
NC_000017.10:g.59533348_59533350delinsCCT , CM000679.1:g.59533348_59533350delinsCCT	GRCh37
NC_000017.9:g.56888130_56888132delinsCCT	NCBI36
NG_008080.1:g.4542_4544delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644296.1:c.-3-501_-3-499delinsCCT MANE Select	ENSP00000495986.1:n.-3-501_-3-499delinsCCT
ENST00000393853.8:c.-3-501_-3-499delinsCCT	ENSP00000377435.3:n.-3-501_-3-499delinsCCT
ENST00000589003.5:c.-125-637_-125-635delinsCCT	ENSP00000467588.1:n.-125-637_-125-635delinsCCT
XM_005257835.3:c.-3-501_-3-499delinsCCT	XP_005257892.2:n.-3-501_-3-499delinsCCT
XM_005257837.2:c.-3-501_-3-499delinsCCT	XP_005257894.1:n.-3-501_-3-499delinsCCT
XM_011525490.1:c.187-501_187-499delinsCCT	XP_011523792.1:n.187-501_187-499delinsCCT
XM_011525491.1:c.187-501_187-499delinsCCT	XP_011523793.1:n.187-501_187-499delinsCCT
XM_011525492.1:c.-3-501_-3-499delinsCCT	XP_011523794.1:n.-3-501_-3-499delinsCCT
XM_011525493.1:c.-3-501_-3-499delinsCCT	XP_011523795.1:n.-3-501_-3-499delinsCCT
XM_011525494.1:c.-4+252_-4+254delinsCCT	XP_011523796.1:n.-4+252_-4+254delinsCCT
XM_011525495.1:c.187-501_187-499delinsCCT	XP_011523797.1:n.187-501_187-499delinsCCT
NM_001321120.2:c.-3-501_-3-499delinsCCT MANE Select	NP_001308049.1:n.-3-501_-3-499delinsCCT
XM_011525490.2:c.187-501_187-499delinsCCT	XP_011523792.1:n.187-501_187-499delinsCCT
XM_011525491.2:c.187-501_187-499delinsCCT	XP_011523793.1:n.187-501_187-499delinsCCT
XM_011525495.2:c.187-501_187-499delinsCCT	XP_011523797.1:n.187-501_187-499delinsCCT