Canonical Allele Identifier: CA386861943

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114836380G>C (hg19) ; chr12:g.114398575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114398575G>C , CM000674.2:g.114398575G>C	GRCh38
NC_000012.11:g.114836380G>C , CM000674.1:g.114836380G>C	GRCh37
NC_000012.10:g.113320763G>C	NCBI36
NG_007373.1:g.14868C>G , LRG_670:g.14868C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.508C>G MANE Select	ENSP00000384152.3:p.His170Asp
ENST00000310346.8:c.508C>G	ENSP00000309913.4:p.His170Asp
ENST00000349716.9:c.358C>G	ENSP00000337723.5:p.His120Asp
ENST00000405440.6:c.508C>G	ENSP00000384152.2:p.His170Asp
ENST00000526441.1:c.508C>G	ENSP00000433292.1:p.His170Asp
ENST00000552726.1:n.559C>G
NM_000192.3:c.508C>G , LRG_670t1:c.508C>G	NP_000183.2:p.His170Asp
NM_080717.2:c.358C>G	NP_542448.1:p.His120Asp
NM_181486.2:c.508C>G	NP_852259.1:p.His170Asp
XM_017019912.1:c.556C>G	XP_016875401.1:p.His186Asp
NM_080717.3:c.358C>G	NP_542448.1:p.His120Asp
NM_181486.4:c.508C>G MANE Select	NP_852259.1:p.His170Asp
NM_080717.4:c.358C>G	NP_542448.1:p.His120Asp