Canonical Allele Identifier: CA2528193818
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114354365C>A , CM000674.2:g.114354365C>A GRCh38
NC_000012.11:g.114792170C>A , CM000674.1:g.114792170C>A GRCh37
NC_000012.10:g.113276553C>A NCBI36
NG_007373.1:g.59078G>T , LRG_670:g.59078G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405440.7:c.*1167G>T MANE Select ENSP00000384152.3:n.*1167G>T
ENST00000310346.8:c.*1167G>T ENSP00000309913.4:n.*1167G>T
ENST00000349716.9:c.*1167G>T ENSP00000337723.5:n.*1167G>T
NM_000192.3:c.*1167G>T , LRG_670t1:c.*1167G>T NP_000183.2:n.*1167G>T
NM_080717.2:c.*1167G>T NP_542448.1:n.*1167G>T
NM_181486.2:c.*1167G>T NP_852259.1:n.*1167G>T
XM_017019912.1:c.*1167G>T XP_016875401.1:n.*1167G>T
NM_080717.3:c.*1167G>T NP_542448.1:n.*1167G>T
NM_181486.4:c.*1167G>T MANE Select NP_852259.1:n.*1167G>T
NM_080717.4:c.*1167G>T NP_542448.1:n.*1167G>T