Canonical Allele Identifier: CA1679782968
Gene: TBXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.166160682G= , CM000668.2:g.166160682G= GRCh38
NC_000006.11:g.166574170G= , CM000668.1:g.166574170G= GRCh37
NC_000006.10:g.166494160G= NCBI36
NG_012135.1:g.12962C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366876.7:c.1037+155C= MANE Select ENSP00000355841.3:n.1037+155C=
ENST00000296946.6:c.1034+155C= ENSP00000296946.2:n.1034+155C=
ENST00000366871.7:c.860+155C= ENSP00000355836.3:n.860+155C=
ENST00000366876.6:c.1037+155C= ENSP00000355841.2:n.1037+155C=
NM_001270484.1:c.860+155C= NP_001257413.1:n.860+155C=
NM_003181.3:c.1034+155C= NP_003172.1:n.1034+155C=
XM_011536080.1:c.1037+155C= XP_011534382.1:n.1037+155C=
XM_011536081.1:c.860+155C= XP_011534383.1:n.860+155C=
NM_001366285.1:c.1037+155C= NP_001353214.1:n.1037+155C=
NM_001366286.1:c.1037+155C= NP_001353215.1:n.1037+155C=
NM_001270484.2:c.860+155C= NP_001257413.1:n.860+155C=
NM_001366285.2:c.1037+155C= MANE Select NP_001353214.1:n.1037+155C=
NM_001366286.2:c.1037+155C= NP_001353215.1:n.1037+155C=
NM_003181.4:c.1034+155C= NP_003172.1:n.1034+155C=