Canonical Allele Identifier: CA386863478

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841589G>T (hg19) ; chr12:g.114403784G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403784G>T , CM000674.2:g.114403784G>T	GRCh38
NC_000012.11:g.114841589G>T , CM000674.1:g.114841589G>T	GRCh37
NC_000012.10:g.113325972G>T	NCBI36
NG_007373.1:g.9659C>A , LRG_670:g.9659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.115C>A MANE Select	ENSP00000384152.3:p.Pro39Thr
ENST00000310346.8:c.115C>A	ENSP00000309913.4:p.Pro39Thr
ENST00000349716.9:c.-3-1864C>A	ENSP00000337723.5:n.-3-1864C>A
ENST00000405440.6:c.115C>A	ENSP00000384152.2:p.Pro39Thr
ENST00000526441.1:c.115C>A	ENSP00000433292.1:p.Pro39Thr
ENST00000552726.1:n.166C>A
NM_000192.3:c.115C>A , LRG_670t1:c.115C>A	NP_000183.2:p.Pro39Thr
NM_080717.2:c.-3-1864C>A	NP_542448.1:n.-3-1864C>A
NM_181486.2:c.115C>A	NP_852259.1:p.Pro39Thr
XM_017019912.1:c.163C>A	XP_016875401.1:p.Pro55Thr
NM_080717.3:c.-3-1864C>A	NP_542448.1:n.-3-1864C>A
NM_181486.4:c.115C>A MANE Select	NP_852259.1:p.Pro39Thr
NM_080717.4:c.-3-1864C>A	NP_542448.1:n.-3-1864C>A