Canonical Allele Identifier: CA386863590

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841645T>G (hg19) ; chr12:g.114403840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403840T>G , CM000674.2:g.114403840T>G	GRCh38
NC_000012.11:g.114841645T>G , CM000674.1:g.114841645T>G	GRCh37
NC_000012.10:g.113326028T>G	NCBI36
NG_007373.1:g.9603A>C , LRG_670:g.9603A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.59A>C MANE Select	ENSP00000384152.3:p.Lys20Thr
ENST00000310346.8:c.59A>C	ENSP00000309913.4:p.Lys20Thr
ENST00000349716.9:c.-3-1920A>C	ENSP00000337723.5:n.-3-1920A>C
ENST00000405440.6:c.59A>C	ENSP00000384152.2:p.Lys20Thr
ENST00000526441.1:c.59A>C	ENSP00000433292.1:p.Lys20Thr
ENST00000552726.1:n.110A>C
NM_000192.3:c.59A>C , LRG_670t1:c.59A>C	NP_000183.2:p.Lys20Thr
NM_080717.2:c.-3-1920A>C	NP_542448.1:n.-3-1920A>C
NM_181486.2:c.59A>C	NP_852259.1:p.Lys20Thr
XM_017019912.1:c.107A>C	XP_016875401.1:p.Lys36Thr
NM_080717.3:c.-3-1920A>C	NP_542448.1:n.-3-1920A>C
NM_181486.4:c.59A>C MANE Select	NP_852259.1:p.Lys20Thr
NM_080717.4:c.-3-1920A>C	NP_542448.1:n.-3-1920A>C