Canonical Allele Identifier: CA386861966

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114836391T>C (hg19) ; chr12:g.114398586T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114398586T>C , CM000674.2:g.114398586T>C	GRCh38
NC_000012.11:g.114836391T>C , CM000674.1:g.114836391T>C	GRCh37
NC_000012.10:g.113320774T>C	NCBI36
NG_007373.1:g.14857A>G , LRG_670:g.14857A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.497A>G MANE Select	ENSP00000384152.3:p.Asp166Gly
ENST00000310346.8:c.497A>G	ENSP00000309913.4:p.Asp166Gly
ENST00000349716.9:c.347A>G	ENSP00000337723.5:p.Asp116Gly
ENST00000405440.6:c.497A>G	ENSP00000384152.2:p.Asp166Gly
ENST00000526441.1:c.497A>G	ENSP00000433292.1:p.Asp166Gly
ENST00000552726.1:n.548A>G
NM_000192.3:c.497A>G , LRG_670t1:c.497A>G	NP_000183.2:p.Asp166Gly
NM_080717.2:c.347A>G	NP_542448.1:p.Asp116Gly
NM_181486.2:c.497A>G	NP_852259.1:p.Asp166Gly
XM_017019912.1:c.545A>G	XP_016875401.1:p.Asp182Gly
NM_080717.3:c.347A>G	NP_542448.1:p.Asp116Gly
NM_181486.4:c.497A>G MANE Select	NP_852259.1:p.Asp166Gly
NM_080717.4:c.347A>G	NP_542448.1:p.Asp116Gly