Canonical Allele Identifier: CA2064632885

Gene: TBX5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114354385_114354386delinsCT , CM000674.2:g.114354385_114354386delinsCT	GRCh38
NC_000012.11:g.114792190_114792191delinsCT , CM000674.1:g.114792190_114792191delinsCT	GRCh37
NC_000012.10:g.113276573_113276574delinsCT	NCBI36
NG_007373.1:g.59057_59058delinsAG , LRG_670:g.59057_59058delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000405440.7:c.*1146_*1147delinsAG MANE Select	ENSP00000384152.3:n.*1146_*1147delinsAG
ENST00000310346.8:c.*1146_*1147delinsAG	ENSP00000309913.4:n.*1146_*1147delinsAG
ENST00000349716.9:c.*1146_*1147delinsAG	ENSP00000337723.5:n.*1146_*1147delinsAG
NM_000192.3:c.*1146_*1147delinsAG , LRG_670t1:c.*1146_*1147delinsAG	NP_000183.2:n.*1146_*1147delinsAG
NM_080717.2:c.*1146_*1147delinsAG	NP_542448.1:n.*1146_*1147delinsAG
NM_181486.2:c.*1146_*1147delinsAG	NP_852259.1:n.*1146_*1147delinsAG
XM_017019912.1:c.*1146_*1147delinsAG	XP_016875401.1:n.*1146_*1147delinsAG
NM_080717.3:c.*1146_*1147delinsAG	NP_542448.1:n.*1146_*1147delinsAG
NM_181486.4:c.*1146_*1147delinsAG MANE Select	NP_852259.1:n.*1146_*1147delinsAG
NM_080717.4:c.*1146_*1147delinsAG	NP_542448.1:n.*1146_*1147delinsAG