Canonical Allele Identifier: CA6809577
Community Standard Title: NM_181486.4(TBX5):c.564G>A (p.Ala188=)
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114394840C>T , CM000674.2:g.114394840C>T GRCh38
NC_000012.11:g.114832645C>T , CM000674.1:g.114832645C>T GRCh37
NC_000012.10:g.113317028C>T NCBI36
NG_007373.1:g.18603G>A , LRG_670:g.18603G>A

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.564G>A MANE Select NP_852259.1:p.Ala188=
ENST00000405440.7:c.564G>A MANE Select ENSP00000384152.3:p.Ala188=
NM_000192.3:c.564G>A , LRG_670t1:c.564G>A NP_000183.2:p.Ala188=
NM_080717.2:c.414G>A NP_542448.1:p.Ala138=
NM_080717.3:c.414G>A NP_542448.1:p.Ala138=
NM_080717.4:c.414G>A NP_542448.1:p.Ala138=
NM_181486.2:c.564G>A NP_852259.1:p.Ala188=
ENST00000310346.8:c.564G>A ENSP00000309913.4:p.Ala188=
ENST00000349716.9:c.414G>A ENSP00000337723.5:p.Ala138=
ENST00000405440.6:c.564G>A ENSP00000384152.2:p.Ala188=
ENST00000526441.1:c.564G>A ENSP00000433292.1:p.Ala188=
XM_017019912.1:c.612G>A XP_016875401.1:p.Ala204=