Canonical Allele Identifier: CA386859678
Community Standard Title: NM_181486.4(TBX5):c.709C>G (p.Arg237Gly)
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114385522G>C , CM000674.2:g.114385522G>C GRCh38
NC_000012.11:g.114823327G>C , CM000674.1:g.114823327G>C GRCh37
NC_000012.10:g.113307710G>C NCBI36
NG_007373.1:g.27921C>G , LRG_670:g.27921C>G

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.709C>G MANE Select NP_852259.1:p.Arg237Gly
ENST00000405440.7:c.709C>G MANE Select ENSP00000384152.3:p.Arg237Gly
NM_000192.3:c.709C>G , LRG_670t1:c.709C>G NP_000183.2:p.Arg237Gly
NM_080717.2:c.559C>G NP_542448.1:p.Arg187Gly
NM_080717.3:c.559C>G NP_542448.1:p.Arg187Gly
NM_080717.4:c.559C>G NP_542448.1:p.Arg187Gly
NM_181486.2:c.709C>G NP_852259.1:p.Arg237Gly
ENST00000310346.8:c.709C>G ENSP00000309913.4:p.Arg237Gly
ENST00000349716.9:c.559C>G ENSP00000337723.5:p.Arg187Gly
ENST00000405440.6:c.709C>G ENSP00000384152.2:p.Arg237Gly
ENST00000526441.1:c.709C>G ENSP00000433292.1:p.Arg237Gly
XM_017019912.1:c.757C>G XP_016875401.1:p.Arg253Gly