Canonical Allele Identifier: CA386863552

Gene: TBX5

Linked Data

• dbSNP Id: rs1085307848
• MyVariant Identifiers: chr12:g.114841627G>C (hg19) ; chr12:g.114403822G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114403822G>C , CM000674.2:g.114403822G>C	GRCh38
NC_000012.11:g.114841627G>C , CM000674.1:g.114841627G>C	GRCh37
NC_000012.10:g.113326010G>C	NCBI36
NG_007373.1:g.9621C>G , LRG_670:g.9621C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405440.7:c.77C>G MANE Select	ENSP00000384152.3:p.Ser26Trp
ENST00000310346.8:c.77C>G	ENSP00000309913.4:p.Ser26Trp
ENST00000349716.9:c.-3-1902C>G	ENSP00000337723.5:n.-3-1902C>G
ENST00000405440.6:c.77C>G	ENSP00000384152.2:p.Ser26Trp
ENST00000526441.1:c.77C>G	ENSP00000433292.1:p.Ser26Trp
ENST00000552726.1:n.128C>G
NM_000192.3:c.77C>G , LRG_670t1:c.77C>G	NP_000183.2:p.Ser26Trp
NM_080717.2:c.-3-1902C>G	NP_542448.1:n.-3-1902C>G
NM_181486.2:c.77C>G	NP_852259.1:p.Ser26Trp
XM_017019912.1:c.125C>G	XP_016875401.1:p.Ser42Trp
NM_080717.3:c.-3-1902C>G	NP_542448.1:n.-3-1902C>G
NM_181486.4:c.77C>G MANE Select	NP_852259.1:p.Ser26Trp
NM_080717.4:c.-3-1902C>G	NP_542448.1:n.-3-1902C>G