Canonical Allele Identifier: CA386863426

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841564G>A (hg19) ; chr12:g.114403759G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403759G>A , CM000674.2:g.114403759G>A	GRCh38
NC_000012.11:g.114841564G>A , CM000674.1:g.114841564G>A	GRCh37
NC_000012.10:g.113325947G>A	NCBI36
NG_007373.1:g.9684C>T , LRG_670:g.9684C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.140C>T MANE Select	ENSP00000384152.3:p.Thr47Ile
ENST00000310346.8:c.140C>T	ENSP00000309913.4:p.Thr47Ile
ENST00000349716.9:c.-3-1839C>T	ENSP00000337723.5:n.-3-1839C>T
ENST00000405440.6:c.140C>T	ENSP00000384152.2:p.Thr47Ile
ENST00000526441.1:c.140C>T	ENSP00000433292.1:p.Thr47Ile
ENST00000552726.1:n.191C>T
NM_000192.3:c.140C>T , LRG_670t1:c.140C>T	NP_000183.2:p.Thr47Ile
NM_080717.2:c.-3-1839C>T	NP_542448.1:n.-3-1839C>T
NM_181486.2:c.140C>T	NP_852259.1:p.Thr47Ile
XM_017019912.1:c.188C>T	XP_016875401.1:p.Thr63Ile
NM_080717.3:c.-3-1839C>T	NP_542448.1:n.-3-1839C>T
NM_181486.4:c.140C>T MANE Select	NP_852259.1:p.Thr47Ile
NM_080717.4:c.-3-1839C>T	NP_542448.1:n.-3-1839C>T