Canonical Allele Identifier: CA386863422

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841561T>C (hg19) ; chr12:g.114403756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403756T>C , CM000674.2:g.114403756T>C	GRCh38
NC_000012.11:g.114841561T>C , CM000674.1:g.114841561T>C	GRCh37
NC_000012.10:g.113325944T>C	NCBI36
NG_007373.1:g.9687A>G , LRG_670:g.9687A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.143A>G MANE Select	ENSP00000384152.3:p.Gln48Arg
ENST00000310346.8:c.143A>G	ENSP00000309913.4:p.Gln48Arg
ENST00000349716.9:c.-3-1836A>G	ENSP00000337723.5:n.-3-1836A>G
ENST00000405440.6:c.143A>G	ENSP00000384152.2:p.Gln48Arg
ENST00000526441.1:c.143A>G	ENSP00000433292.1:p.Gln48Arg
ENST00000552726.1:n.194A>G
NM_000192.3:c.143A>G , LRG_670t1:c.143A>G	NP_000183.2:p.Gln48Arg
NM_080717.2:c.-3-1836A>G	NP_542448.1:n.-3-1836A>G
NM_181486.2:c.143A>G	NP_852259.1:p.Gln48Arg
XM_017019912.1:c.191A>G	XP_016875401.1:p.Gln64Arg
NM_080717.3:c.-3-1836A>G	NP_542448.1:n.-3-1836A>G
NM_181486.4:c.143A>G MANE Select	NP_852259.1:p.Gln48Arg
NM_080717.4:c.-3-1836A>G	NP_542448.1:n.-3-1836A>G