Canonical Allele Identifier: CA913191206

Gene: TBX5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114401821C>T , CM000674.2:g.114401821C>T	GRCh38
NC_000012.11:g.114839626C>T , CM000674.1:g.114839626C>T	GRCh37
NC_000012.10:g.113324009C>T	NCBI36
NG_007373.1:g.11622G>A , LRG_670:g.11622G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181486.4:c.242+5G>A MANE Select	NP_852259.1:n.242+5G>A
ENST00000405440.7:c.242+5G>A MANE Select	ENSP00000384152.3:n.242+5G>A
NM_000192.3:c.242+5G>A , LRG_670t1:c.242+5G>A	NP_000183.2:n.242+5G>A
NM_080717.2:c.92+5G>A	NP_542448.1:n.92+5G>A
NM_080717.3:c.92+5G>A	NP_542448.1:n.92+5G>A
NM_080717.4:c.92+5G>A	NP_542448.1:n.92+5G>A
NM_181486.2:c.242+5G>A	NP_852259.1:n.242+5G>A
ENST00000310346.8:c.242+5G>A	ENSP00000309913.4:n.242+5G>A
ENST00000349716.9:c.92+5G>A	ENSP00000337723.5:n.92+5G>A
ENST00000405440.6:c.242+5G>A	ENSP00000384152.2:n.242+5G>A
ENST00000526441.1:c.242+5G>A	ENSP00000433292.1:n.242+5G>A
ENST00000552726.1:n.293+5G>A
XM_017019912.1:c.290+5G>A	XP_016875401.1:n.290+5G>A