Canonical Allele Identifier: CA2797548250
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114354871G>A , CM000674.2:g.114354871G>A GRCh38
NC_000012.11:g.114792676G>A , CM000674.1:g.114792676G>A GRCh37
NC_000012.10:g.113277059G>A NCBI36
NG_007373.1:g.58572C>T , LRG_670:g.58572C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405440.7:c.*661C>T MANE Select ENSP00000384152.3:n.*661C>T
ENST00000310346.8:c.*661C>T ENSP00000309913.4:n.*661C>T
ENST00000349716.9:c.*661C>T ENSP00000337723.5:n.*661C>T
NM_000192.3:c.*661C>T , LRG_670t1:c.*661C>T NP_000183.2:n.*661C>T
NM_080717.2:c.*661C>T NP_542448.1:n.*661C>T
NM_181486.2:c.*661C>T NP_852259.1:n.*661C>T
XM_017019912.1:c.*661C>T XP_016875401.1:n.*661C>T
NM_080717.3:c.*661C>T NP_542448.1:n.*661C>T
NM_181486.4:c.*661C>T MANE Select NP_852259.1:n.*661C>T
NM_080717.4:c.*661C>T NP_542448.1:n.*661C>T