Canonical Allele Identifier: CA16456275

Gene: TBX5

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114357638G>A , CM000674.2:g.114357638G>A	GRCh38
NC_000012.11:g.114795443G>A , CM000674.1:g.114795443G>A	GRCh37
NC_000012.10:g.113279826G>A	NCBI36
NG_007373.1:g.55805C>T , LRG_670:g.55805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.983-1532C>T MANE Select	ENSP00000384152.3:n.983-1532C>T
ENST00000310346.8:c.983-1532C>T	ENSP00000309913.4:n.983-1532C>T
ENST00000349716.9:c.833-1532C>T	ENSP00000337723.5:n.833-1532C>T
ENST00000405440.6:c.983-1532C>T	ENSP00000384152.2:n.983-1532C>T
NM_000192.3:c.983-1532C>T , LRG_670t1:c.983-1532C>T	NP_000183.2:n.983-1532C>T
NM_080717.2:c.833-1532C>T	NP_542448.1:n.833-1532C>T
NM_181486.2:c.983-1532C>T	NP_852259.1:n.983-1532C>T
XM_017019912.1:c.1031-1532C>T	XP_016875401.1:n.1031-1532C>T
NM_080717.3:c.833-1532C>T	NP_542448.1:n.833-1532C>T
NM_181486.4:c.983-1532C>T MANE Select	NP_852259.1:n.983-1532C>T
NM_080717.4:c.833-1532C>T	NP_542448.1:n.833-1532C>T