Canonical Allele Identifier: CA10641040
Community Standard Title: NM_181486.4(TBX5):c.846C>T (p.Ser282=)
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114366301G>A , CM000674.2:g.114366301G>A GRCh38
NC_000012.11:g.114804106G>A , CM000674.1:g.114804106G>A GRCh37
NC_000012.10:g.113288489G>A NCBI36
NG_007373.1:g.47142C>T , LRG_670:g.47142C>T

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.846C>T MANE Select NP_852259.1:p.Ser282=
ENST00000405440.7:c.846C>T MANE Select ENSP00000384152.3:p.Ser282=
NM_000192.3:c.846C>T , LRG_670t1:c.846C>T NP_000183.2:p.Ser282=
NM_080717.2:c.696C>T NP_542448.1:p.Ser232=
NM_080717.3:c.696C>T NP_542448.1:p.Ser232=
NM_080717.4:c.696C>T NP_542448.1:p.Ser232=
NM_181486.2:c.846C>T NP_852259.1:p.Ser282=
ENST00000310346.8:c.846C>T ENSP00000309913.4:p.Ser282=
ENST00000349716.9:c.696C>T ENSP00000337723.5:p.Ser232=
ENST00000405440.6:c.846C>T ENSP00000384152.2:p.Ser282=
ENST00000526441.1:c.846C>T ENSP00000433292.1:p.Ser282=
XM_017019912.1:c.894C>T XP_016875401.1:p.Ser298=