Canonical Allele Identifier: CA481920952

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114841605C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403800C>G , CM000674.2:g.114403800C>G	GRCh38
NC_000012.11:g.114841605C>G , CM000674.1:g.114841605C>G	GRCh37
NC_000012.10:g.113325988C>G	NCBI36
NG_007373.1:g.9643G>C , LRG_670:g.9643G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.99G>C MANE Select	ENSP00000384152.3:p.Gly33=
ENST00000310346.8:c.99G>C	ENSP00000309913.4:p.Gly33=
ENST00000349716.9:c.-3-1880G>C	ENSP00000337723.5:n.-3-1880G>C
ENST00000405440.6:c.99G>C	ENSP00000384152.2:p.Gly33=
ENST00000526441.1:c.99G>C	ENSP00000433292.1:p.Gly33=
ENST00000552726.1:n.150G>C
NM_000192.3:c.99G>C , LRG_670t1:c.99G>C	NP_000183.2:p.Gly33=
NM_080717.2:c.-3-1880G>C	NP_542448.1:n.-3-1880G>C
NM_181486.2:c.99G>C	NP_852259.1:p.Gly33=
XM_017019912.1:c.147G>C	XP_016875401.1:p.Gly49=
NM_080717.3:c.-3-1880G>C	NP_542448.1:n.-3-1880G>C
NM_181486.4:c.99G>C MANE Select	NP_852259.1:p.Gly33=
NM_080717.4:c.-3-1880G>C	NP_542448.1:n.-3-1880G>C