Canonical Allele Identifier: CA2064633117
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114354901G= , CM000674.2:g.114354901G= GRCh38
NC_000012.11:g.114792706G= , CM000674.1:g.114792706G= GRCh37
NC_000012.10:g.113277089G= NCBI36
NG_007373.1:g.58542C= , LRG_670:g.58542C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.*631C= MANE Select ENSP00000384152.3:n.*631C=
ENST00000310346.8:c.*631C= ENSP00000309913.4:n.*631C=
ENST00000349716.9:c.*631C= ENSP00000337723.5:n.*631C=
NM_000192.3:c.*631C= , LRG_670t1:c.*631C= NP_000183.2:n.*631C=
NM_080717.2:c.*631C= NP_542448.1:n.*631C=
NM_181486.2:c.*631C= NP_852259.1:n.*631C=
XM_017019912.1:c.*631C= XP_016875401.1:n.*631C=
NM_080717.3:c.*631C= NP_542448.1:n.*631C=
NM_181486.4:c.*631C= MANE Select NP_852259.1:n.*631C=
NM_080717.4:c.*631C= NP_542448.1:n.*631C=