Canonical Allele Identifier: CA2621125324

Gene: TBX5

Linked Data

• gnomAD v4: 12-114399493-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114399493C>T , CM000674.2:g.114399493C>T	GRCh38
NC_000012.11:g.114837298C>T , CM000674.1:g.114837298C>T	GRCh37
NC_000012.10:g.113321681C>T	NCBI36
NG_007373.1:g.13950G>A , LRG_670:g.13950G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.362+20G>A MANE Select	ENSP00000384152.3:n.362+20G>A
ENST00000310346.8:c.362+20G>A	ENSP00000309913.4:n.362+20G>A
ENST00000349716.9:c.212+20G>A	ENSP00000337723.5:n.212+20G>A
ENST00000405440.6:c.362+20G>A	ENSP00000384152.2:n.362+20G>A
ENST00000526441.1:c.362+20G>A	ENSP00000433292.1:n.362+20G>A
ENST00000552726.1:n.413+20G>A
NM_000192.3:c.362+20G>A , LRG_670t1:c.362+20G>A	NP_000183.2:n.362+20G>A
NM_080717.2:c.212+20G>A	NP_542448.1:n.212+20G>A
NM_181486.2:c.362+20G>A	NP_852259.1:n.362+20G>A
XM_017019912.1:c.410+20G>A	XP_016875401.1:n.410+20G>A
NM_080717.3:c.212+20G>A	NP_542448.1:n.212+20G>A
NM_181486.4:c.362+20G>A MANE Select	NP_852259.1:n.362+20G>A
NM_080717.4:c.212+20G>A	NP_542448.1:n.212+20G>A