Canonical Allele Identifier: CA2064659056
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114403827G= , CM000674.2:g.114403827G= GRCh38
NC_000012.11:g.114841632G= , CM000674.1:g.114841632G= GRCh37
NC_000012.10:g.113326015G= NCBI36
NG_007373.1:g.9616C= , LRG_670:g.9616C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.72C= MANE Select ENSP00000384152.3:p.Cys24=
ENST00000310346.8:c.72C= ENSP00000309913.4:p.Cys24=
ENST00000349716.9:c.-3-1907C= ENSP00000337723.5:n.-3-1907C=
ENST00000405440.6:c.72C= ENSP00000384152.2:p.Cys24=
ENST00000526441.1:c.72C= ENSP00000433292.1:p.Cys24=
ENST00000552726.1:n.123C=
NM_000192.3:c.72C= , LRG_670t1:c.72C= NP_000183.2:p.Cys24=
NM_080717.2:c.-3-1907C= NP_542448.1:n.-3-1907C=
NM_181486.2:c.72C= NP_852259.1:p.Cys24=
XM_017019912.1:c.120C= XP_016875401.1:p.Cys40=
NM_080717.3:c.-3-1907C= NP_542448.1:n.-3-1907C=
NM_181486.4:c.72C= MANE Select NP_852259.1:p.Cys24=
NM_080717.4:c.-3-1907C= NP_542448.1:n.-3-1907C=