Canonical Allele Identifier: CA16042869
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114385521C>G , CM000674.2:g.114385521C>G GRCh38
NC_000012.11:g.114823326C>G , CM000674.1:g.114823326C>G GRCh37
NC_000012.10:g.113307709C>G NCBI36
NG_007373.1:g.27922G>C , LRG_670:g.27922G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.710G>C MANE Select ENSP00000384152.3:p.Arg237Pro
ENST00000310346.8:c.710G>C ENSP00000309913.4:p.Arg237Pro
ENST00000349716.9:c.560G>C ENSP00000337723.5:p.Arg187Pro
ENST00000405440.6:c.710G>C ENSP00000384152.2:p.Arg237Pro
ENST00000526441.1:c.710G>C ENSP00000433292.1:p.Arg237Pro
NM_000192.3:c.710G>C , LRG_670t1:c.710G>C NP_000183.2:p.Arg237Pro
NM_080717.2:c.560G>C NP_542448.1:p.Arg187Pro
NM_181486.2:c.710G>C NP_852259.1:p.Arg237Pro
XM_017019912.1:c.758G>C XP_016875401.1:p.Arg253Pro
NM_080717.3:c.560G>C NP_542448.1:p.Arg187Pro
NM_181486.4:c.710G>C MANE Select NP_852259.1:p.Arg237Pro
NM_080717.4:c.560G>C NP_542448.1:p.Arg187Pro