Canonical Allele Identifier: CA2064638473
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114366312G= , CM000674.2:g.114366312G= GRCh38
NC_000012.11:g.114804117G= , CM000674.1:g.114804117G= GRCh37
NC_000012.10:g.113288500G= NCBI36
NG_007373.1:g.47131C= , LRG_670:g.47131C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.835C= MANE Select ENSP00000384152.3:p.Arg279=
ENST00000310346.8:c.835C= ENSP00000309913.4:p.Arg279=
ENST00000349716.9:c.685C= ENSP00000337723.5:p.Arg229=
ENST00000405440.6:c.835C= ENSP00000384152.2:p.Arg279=
ENST00000526441.1:c.835C= ENSP00000433292.1:p.Arg279=
NM_000192.3:c.835C= , LRG_670t1:c.835C= NP_000183.2:p.Arg279=
NM_080717.2:c.685C= NP_542448.1:p.Arg229=
NM_181486.2:c.835C= NP_852259.1:p.Arg279=
XM_017019912.1:c.883C= XP_016875401.1:p.Arg295=
NM_080717.3:c.685C= NP_542448.1:p.Arg229=
NM_181486.4:c.835C= MANE Select NP_852259.1:p.Arg279=
NM_080717.4:c.685C= NP_542448.1:p.Arg229=