Canonical Allele Identifier: CA2621125106

Gene: TBX5

Linked Data

• gnomAD v4: 12-114398566-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114398566T>G , CM000674.2:g.114398566T>G	GRCh38
NC_000012.11:g.114836371T>G , CM000674.1:g.114836371T>G	GRCh37
NC_000012.10:g.113320754T>G	NCBI36
NG_007373.1:g.14877A>C , LRG_670:g.14877A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.510+7A>C MANE Select	ENSP00000384152.3:n.510+7A>C
ENST00000310346.8:c.510+7A>C	ENSP00000309913.4:n.510+7A>C
ENST00000349716.9:c.360+7A>C	ENSP00000337723.5:n.360+7A>C
ENST00000405440.6:c.510+7A>C	ENSP00000384152.2:n.510+7A>C
ENST00000526441.1:c.510+7A>C	ENSP00000433292.1:n.510+7A>C
ENST00000552726.1:n.561+7A>C
NM_000192.3:c.510+7A>C , LRG_670t1:c.510+7A>C	NP_000183.2:n.510+7A>C
NM_080717.2:c.360+7A>C	NP_542448.1:n.360+7A>C
NM_181486.2:c.510+7A>C	NP_852259.1:n.510+7A>C
XM_017019912.1:c.558+7A>C	XP_016875401.1:n.558+7A>C
NM_080717.3:c.360+7A>C	NP_542448.1:n.360+7A>C
NM_181486.4:c.510+7A>C MANE Select	NP_852259.1:n.510+7A>C
NM_080717.4:c.360+7A>C	NP_542448.1:n.360+7A>C