Canonical Allele Identifier: CA1630855787
Community Standard Title: NM_181486.4(TBX5):c.*97G=
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114355435C= , CM000674.2:g.114355435C= GRCh38
NC_000012.11:g.114793240C= , CM000674.1:g.114793240C= GRCh37
NC_000012.10:g.113277623C= NCBI36
NG_007373.1:g.58008G= , LRG_670:g.58008G=

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.*97G= MANE Select NP_852259.1:n.*97G=
ENST00000405440.7:c.*97G= MANE Select ENSP00000384152.3:n.*97G=
NM_000192.3:c.*97G= , LRG_670t1:c.*97G= NP_000183.2:n.*97G=
NM_080717.2:c.*97G= NP_542448.1:n.*97G=
NM_080717.3:c.*97G= NP_542448.1:n.*97G=
NM_080717.4:c.*97G= NP_542448.1:n.*97G=
NM_181486.2:c.*97G= NP_852259.1:n.*97G=
ENST00000310346.8:c.*97G= ENSP00000309913.4:n.*97G=
ENST00000349716.9:c.*97G= ENSP00000337723.5:n.*97G=
ENST00000405440.6:c.*97G= ENSP00000384152.2:n.*97G=
XM_017019912.1:c.*97G= XP_016875401.1:n.*97G=