Canonical Allele Identifier: CA386863466

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841582G>T (hg19) ; chr12:g.114403777G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403777G>T , CM000674.2:g.114403777G>T	GRCh38
NC_000012.11:g.114841582G>T , CM000674.1:g.114841582G>T	GRCh37
NC_000012.10:g.113325965G>T	NCBI36
NG_007373.1:g.9666C>A , LRG_670:g.9666C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.122C>A MANE Select	ENSP00000384152.3:p.Ser41Tyr
ENST00000310346.8:c.122C>A	ENSP00000309913.4:p.Ser41Tyr
ENST00000349716.9:c.-3-1857C>A	ENSP00000337723.5:n.-3-1857C>A
ENST00000405440.6:c.122C>A	ENSP00000384152.2:p.Ser41Tyr
ENST00000526441.1:c.122C>A	ENSP00000433292.1:p.Ser41Tyr
ENST00000552726.1:n.173C>A
NM_000192.3:c.122C>A , LRG_670t1:c.122C>A	NP_000183.2:p.Ser41Tyr
NM_080717.2:c.-3-1857C>A	NP_542448.1:n.-3-1857C>A
NM_181486.2:c.122C>A	NP_852259.1:p.Ser41Tyr
XM_017019912.1:c.170C>A	XP_016875401.1:p.Ser57Tyr
NM_080717.3:c.-3-1857C>A	NP_542448.1:n.-3-1857C>A
NM_181486.4:c.122C>A MANE Select	NP_852259.1:p.Ser41Tyr
NM_080717.4:c.-3-1857C>A	NP_542448.1:n.-3-1857C>A