Canonical Allele Identifier: CA2064648280
Community Standard Title: NM_181486.4(TBX5):c.710G= (p.Arg237=)
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114385521C= , CM000674.2:g.114385521C= GRCh38
NC_000012.11:g.114823326C= , CM000674.1:g.114823326C= GRCh37
NC_000012.10:g.113307709C= NCBI36
NG_007373.1:g.27922G= , LRG_670:g.27922G=

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.710G= MANE Select NP_852259.1:p.Arg237=
ENST00000405440.7:c.710G= MANE Select ENSP00000384152.3:p.Arg237=
NM_000192.3:c.710G= , LRG_670t1:c.710G= NP_000183.2:p.Arg237=
NM_080717.2:c.560G= NP_542448.1:p.Arg187=
NM_080717.3:c.560G= NP_542448.1:p.Arg187=
NM_080717.4:c.560G= NP_542448.1:p.Arg187=
NM_181486.2:c.710G= NP_852259.1:p.Arg237=
ENST00000310346.8:c.710G= ENSP00000309913.4:p.Arg237=
ENST00000349716.9:c.560G= ENSP00000337723.5:p.Arg187=
ENST00000405440.6:c.710G= ENSP00000384152.2:p.Arg237=
ENST00000526441.1:c.710G= ENSP00000433292.1:p.Arg237=
XM_017019912.1:c.758G= XP_016875401.1:p.Arg253=