Canonical Allele Identifier: CA386862172

Gene: TBX5

Linked Data

• ClinVar Variation Id: 1716014
• ClinVar RCV Id: RCV002303177
• MyVariant Identifiers: chr12:g.114836487C>G (hg19) ; chr12:g.114398682C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114398682C>G , CM000674.2:g.114398682C>G	GRCh38
NC_000012.11:g.114836487C>G , CM000674.1:g.114836487C>G	GRCh37
NC_000012.10:g.113320870C>G	NCBI36
NG_007373.1:g.14761G>C , LRG_670:g.14761G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.401G>C MANE Select	ENSP00000384152.3:p.Arg134Pro
ENST00000310346.8:c.401G>C	ENSP00000309913.4:p.Arg134Pro
ENST00000349716.9:c.251G>C	ENSP00000337723.5:p.Arg84Pro
ENST00000405440.6:c.401G>C	ENSP00000384152.2:p.Arg134Pro
ENST00000526441.1:c.401G>C	ENSP00000433292.1:p.Arg134Pro
ENST00000552726.1:n.452G>C
NM_000192.3:c.401G>C , LRG_670t1:c.401G>C	NP_000183.2:p.Arg134Pro
NM_080717.2:c.251G>C	NP_542448.1:p.Arg84Pro
NM_181486.2:c.401G>C	NP_852259.1:p.Arg134Pro
XM_017019912.1:c.449G>C	XP_016875401.1:p.Arg150Pro
NM_080717.3:c.251G>C	NP_542448.1:p.Arg84Pro
NM_181486.4:c.401G>C MANE Select	NP_852259.1:p.Arg134Pro
NM_080717.4:c.251G>C	NP_542448.1:p.Arg84Pro