Canonical Allele Identifier: CA2064633281
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114355257T= , CM000674.2:g.114355257T= GRCh38
NC_000012.11:g.114793062T= , CM000674.1:g.114793062T= GRCh37
NC_000012.10:g.113277445T= NCBI36
NG_007373.1:g.58186A= , LRG_670:g.58186A=

Transcript Alleles

HGVS Amino-acid change
ENST00000405440.7:c.*275A= MANE Select ENSP00000384152.3:n.*275A=
ENST00000310346.8:c.*275A= ENSP00000309913.4:n.*275A=
ENST00000349716.9:c.*275A= ENSP00000337723.5:n.*275A=
NM_000192.3:c.*275A= , LRG_670t1:c.*275A= NP_000183.2:n.*275A=
NM_080717.2:c.*275A= NP_542448.1:n.*275A=
NM_181486.2:c.*275A= NP_852259.1:n.*275A=
XM_017019912.1:c.*275A= XP_016875401.1:n.*275A=
NM_080717.3:c.*275A= NP_542448.1:n.*275A=
NM_181486.4:c.*275A= MANE Select NP_852259.1:n.*275A=
NM_080717.4:c.*275A= NP_542448.1:n.*275A=