Canonical Allele Identifier: CA2838956297
Gene: TBX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674773dup , CM000674.2:g.114674773dup GRCh38
NC_000012.11:g.115112578dup , CM000674.1:g.115112578dup GRCh37
NC_000012.10:g.113596961dup NCBI36
NG_008315.1:g.14392dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1102dup MANE Select ENSP00000257567.2:p.Glu368GlyfsTer19
ENST00000257566.7:c.1162dup ENSP00000257566.3:p.Glu388GlyfsTer19
ENST00000349155.6:c.1102dup ENSP00000257567.2:p.Glu368GlyfsTer19
ENST00000613550.1:c.1102dup ENSP00000480048.1:p.Glu368GlyfsTer19
NM_005996.3:c.1102dup NP_005987.3:p.Glu368GlyfsTer19
NM_016569.3:c.1162dup NP_057653.3:p.Glu388GlyfsTer19
NM_005996.4:c.1102dup MANE Select NP_005987.3:p.Glu368GlyfsTer19
NM_016569.4:c.1162dup NP_057653.3:p.Glu388GlyfsTer19
Search 100 bp 5'
Search 100 bp 3'