Canonical Allele Identifier: CA386925820
Community Standard Title: NM_181486.4(TBX5):c.1084C>T (p.Gln362Ter)
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114356005G>A , CM000674.2:g.114356005G>A GRCh38
NC_000012.11:g.114793810G>A , CM000674.1:g.114793810G>A GRCh37
NC_000012.10:g.113278193G>A NCBI36
NG_007373.1:g.57438C>T , LRG_670:g.57438C>T

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.1084C>T MANE Select NP_852259.1:p.Gln362Ter
ENST00000405440.7:c.1084C>T MANE Select ENSP00000384152.3:p.Gln362Ter
NM_000192.3:c.1084C>T , LRG_670t1:c.1084C>T NP_000183.2:p.Gln362Ter
NM_080717.2:c.934C>T NP_542448.1:p.Gln312Ter
NM_080717.3:c.934C>T NP_542448.1:p.Gln312Ter
NM_080717.4:c.934C>T NP_542448.1:p.Gln312Ter
NM_181486.2:c.1084C>T NP_852259.1:p.Gln362Ter
ENST00000310346.8:c.1084C>T ENSP00000309913.4:p.Gln362Ter
ENST00000349716.9:c.934C>T ENSP00000337723.5:p.Gln312Ter
ENST00000405440.6:c.1084C>T ENSP00000384152.2:p.Gln362Ter
XM_017019912.1:c.1132C>T XP_016875401.1:p.Gln378Ter