Canonical Allele Identifier: CA2797548261
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114355010C>G , CM000674.2:g.114355010C>G GRCh38
NC_000012.11:g.114792815C>G , CM000674.1:g.114792815C>G GRCh37
NC_000012.10:g.113277198C>G NCBI36
NG_007373.1:g.58433G>C , LRG_670:g.58433G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.*522G>C MANE Select ENSP00000384152.3:n.*522G>C
ENST00000310346.8:c.*522G>C ENSP00000309913.4:n.*522G>C
ENST00000349716.9:c.*522G>C ENSP00000337723.5:n.*522G>C
NM_000192.3:c.*522G>C , LRG_670t1:c.*522G>C NP_000183.2:n.*522G>C
NM_080717.2:c.*522G>C NP_542448.1:n.*522G>C
NM_181486.2:c.*522G>C NP_852259.1:n.*522G>C
XM_017019912.1:c.*522G>C XP_016875401.1:n.*522G>C
NM_080717.3:c.*522G>C NP_542448.1:n.*522G>C
NM_181486.4:c.*522G>C MANE Select NP_852259.1:n.*522G>C
NM_080717.4:c.*522G>C NP_542448.1:n.*522G>C