Canonical Allele Identifier: CA2064658931

Gene: TBX5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403800C= , CM000674.2:g.114403800C=	GRCh38
NC_000012.11:g.114841605C= , CM000674.1:g.114841605C=	GRCh37
NC_000012.10:g.113325988C=	NCBI36
NG_007373.1:g.9643G= , LRG_670:g.9643G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.99G= MANE Select	ENSP00000384152.3:p.Gly33=
ENST00000310346.8:c.99G=	ENSP00000309913.4:p.Gly33=
ENST00000349716.9:c.-3-1880G=	ENSP00000337723.5:n.-3-1880G=
ENST00000405440.6:c.99G=	ENSP00000384152.2:p.Gly33=
ENST00000526441.1:c.99G=	ENSP00000433292.1:p.Gly33=
ENST00000552726.1:n.150G=
NM_000192.3:c.99G= , LRG_670t1:c.99G=	NP_000183.2:p.Gly33=
NM_080717.2:c.-3-1880G=	NP_542448.1:n.-3-1880G=
NM_181486.2:c.99G=	NP_852259.1:p.Gly33=
XM_017019912.1:c.147G=	XP_016875401.1:p.Gly49=
NM_080717.3:c.-3-1880G=	NP_542448.1:n.-3-1880G=
NM_181486.4:c.99G= MANE Select	NP_852259.1:p.Gly33=
NM_080717.4:c.-3-1880G=	NP_542448.1:n.-3-1880G=