Canonical Allele Identifier: CA627146400
Gene: TBX4 HGNC NCBI

Linked Data

dbSNP Id: rs1482774919

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61456654_61456656del , CM000679.2:g.61456654_61456656del GRCh38
NC_000017.10:g.59534015_59534017del , CM000679.1:g.59534015_59534017del GRCh37
NC_000017.9:g.56888797_56888799del NCBI36
NG_008080.1:g.5209_5211del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642491.1:c.164_166del ENSP00000495714.1:p.Val55del
ENST00000644296.1:c.164_166del MANE Select ENSP00000495986.1:p.Val55del
ENST00000240335.1:c.164_166del ENSP00000240335.1:p.Val55del
ENST00000393853.8:c.164_166del ENSP00000377435.3:p.Val55del
ENST00000589003.5:c.-95_-93del ENSP00000467588.1:n.-95_-93del
NM_018488.2:c.164_166del NP_060958.2:p.Val55del
XM_005257835.3:c.164_166del XP_005257892.2:p.Val55del
XM_005257837.2:c.164_166del XP_005257894.1:p.Val55del
XM_011525490.1:c.353_355del XP_011523792.1:p.Val118del
XM_011525491.1:c.353_355del XP_011523793.1:p.Val118del
XM_011525492.1:c.164_166del XP_011523794.1:p.Val55del
XM_011525493.1:c.164_166del XP_011523795.1:p.Val55del
XM_011525494.1:c.164_166del XP_011523796.1:p.Val55del
XM_011525495.1:c.353_355del XP_011523797.1:p.Val118del
NM_001321120.2:c.164_166del MANE Select NP_001308049.1:p.Val55del
NM_018488.3:c.164_166del NP_060958.2:p.Val55del
XM_011525490.2:c.353_355del XP_011523792.1:p.Val118del
XM_011525491.2:c.353_355del XP_011523793.1:p.Val118del
XM_011525495.2:c.353_355del XP_011523797.1:p.Val118del