Canonical Allele Identifier: CA2537618433

Gene: TBX5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114354392_114354393insTTA , CM000674.2:g.114354392_114354393insTTA	GRCh38
NC_000012.11:g.114792197_114792198insTTA , CM000674.1:g.114792197_114792198insTTA	GRCh37
NC_000012.10:g.113276580_113276581insTTA	NCBI36
NG_007373.1:g.59050_59051insTAA , LRG_670:g.59050_59051insTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.*1139_*1140insTAA MANE Select	ENSP00000384152.3:n.*1139_*1140insTAA
ENST00000310346.8:c.*1139_*1140insTAA	ENSP00000309913.4:n.*1139_*1140insTAA
ENST00000349716.9:c.*1139_*1140insTAA	ENSP00000337723.5:n.*1139_*1140insTAA
NM_000192.3:c.*1139_*1140insTAA , LRG_670t1:c.*1139_*1140insTAA	NP_000183.2:n.*1139_*1140insTAA
NM_080717.2:c.*1139_*1140insTAA	NP_542448.1:n.*1139_*1140insTAA
NM_181486.2:c.*1139_*1140insTAA	NP_852259.1:n.*1139_*1140insTAA
XM_017019912.1:c.*1139_*1140insTAA	XP_016875401.1:n.*1139_*1140insTAA
NM_080717.3:c.*1139_*1140insTAA	NP_542448.1:n.*1139_*1140insTAA
NM_181486.4:c.*1139_*1140insTAA MANE Select	NP_852259.1:n.*1139_*1140insTAA
NM_080717.4:c.*1139_*1140insTAA	NP_542448.1:n.*1139_*1140insTAA