Canonical Allele Identifier: CA2064633170
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114355015A= , CM000674.2:g.114355015A= GRCh38
NC_000012.11:g.114792820A= , CM000674.1:g.114792820A= GRCh37
NC_000012.10:g.113277203A= NCBI36
NG_007373.1:g.58428T= , LRG_670:g.58428T=

Transcript Alleles

HGVS Amino-acid change
ENST00000405440.7:c.*517T= MANE Select ENSP00000384152.3:n.*517T=
ENST00000310346.8:c.*517T= ENSP00000309913.4:n.*517T=
ENST00000349716.9:c.*517T= ENSP00000337723.5:n.*517T=
NM_000192.3:c.*517T= , LRG_670t1:c.*517T= NP_000183.2:n.*517T=
NM_080717.2:c.*517T= NP_542448.1:n.*517T=
NM_181486.2:c.*517T= NP_852259.1:n.*517T=
XM_017019912.1:c.*517T= XP_016875401.1:n.*517T=
NM_080717.3:c.*517T= NP_542448.1:n.*517T=
NM_181486.4:c.*517T= MANE Select NP_852259.1:n.*517T=
NM_080717.4:c.*517T= NP_542448.1:n.*517T=