Canonical Allele Identifier: CA386863232

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114839698G>C (hg19) ; chr12:g.114401893G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114401893G>C , CM000674.2:g.114401893G>C	GRCh38
NC_000012.11:g.114839698G>C , CM000674.1:g.114839698G>C	GRCh37
NC_000012.10:g.113324081G>C	NCBI36
NG_007373.1:g.11550C>G , LRG_670:g.11550C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405440.7:c.175C>G MANE Select	ENSP00000384152.3:p.His59Asp
ENST00000310346.8:c.175C>G	ENSP00000309913.4:p.His59Asp
ENST00000349716.9:c.25C>G	ENSP00000337723.5:p.His9Asp
ENST00000405440.6:c.175C>G	ENSP00000384152.2:p.His59Asp
ENST00000526441.1:c.175C>G	ENSP00000433292.1:p.His59Asp
ENST00000552726.1:n.226C>G
NM_000192.3:c.175C>G , LRG_670t1:c.175C>G	NP_000183.2:p.His59Asp
NM_080717.2:c.25C>G	NP_542448.1:p.His9Asp
NM_181486.2:c.175C>G	NP_852259.1:p.His59Asp
XM_017019912.1:c.223C>G	XP_016875401.1:p.His75Asp
NM_080717.3:c.25C>G	NP_542448.1:p.His9Asp
NM_181486.4:c.175C>G MANE Select	NP_852259.1:p.His59Asp
NM_080717.4:c.25C>G	NP_542448.1:p.His9Asp