Canonical Allele Identifier: CA1747341158
Gene: TBXAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.139962231C= , CM000669.2:g.139962231C= GRCh38
NC_000007.13:g.139662030C= , CM000669.1:g.139662030C= GRCh37
NC_000007.12:g.139308499C= NCBI36
NG_008422.2:g.188850C= , LRG_579:g.188850C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336425.10:c.1132C= ENSP00000338087.7:p.His378=
ENST00000411653.6:c.1132C= ENSP00000411326.3:p.His378=
ENST00000422328.6:c.*921C= ENSP00000415892.3:n.*921C=
ENST00000448866.7:c.1132C= MANE Select ENSP00000402536.3:p.His378=
ENST00000458722.6:c.1270C= ENSP00000411274.3:p.His424=
ENST00000650822.1:c.1135C= ENSP00000498517.1:p.His379=
ENST00000652056.1:c.1135C= ENSP00000498271.1:p.His379=
ENST00000263552.10:c.1135C= ENSP00000263552.6:p.His379=
ENST00000336425.9:c.1132C= ENSP00000338087.5:p.His378=
ENST00000411653.5:c.1132C= ENSP00000411326.1:p.His378=
ENST00000414508.6:c.1135C= ENSP00000392702.2:p.His379=
ENST00000416849.6:c.1273C= ENSP00000389414.2:p.His425=
ENST00000422328.5:c.*921C= ENSP00000415892.1:n.*921C=
ENST00000425687.5:c.931C= ENSP00000388736.1:p.His311=
ENST00000448866.5:c.1132C= ENSP00000402536.1:p.His378=
ENST00000458722.5:c.1270C= ENSP00000411274.1:p.His424=
ENST00000462275.5:n.1103C=
ENST00000469630.1:n.615C=
ENST00000494876.1:n.497C=
NM_001061.4:c.1135C= NP_001052.2:p.His379=
NM_001130966.2:c.1135C= , LRG_579t1:c.1135C= NP_001124438.1:p.His379=
NM_001166253.1:c.1273C= , LRG_579t4:c.1273C= NP_001159725.1:p.His425=
NM_001166254.1:c.931C= , LRG_579t3:c.931C= NP_001159726.1:p.His311=
NM_001314028.1:c.1075C= NP_001300957.1:p.His359=
NM_030984.3:c.1135C= , LRG_579t2:c.1135C= NP_112246.2:p.His379=
NR_029394.1:c.-4294965897C=
XM_011516544.1:c.1135C= XP_011514846.1:p.His379=
NM_001061.5:c.1132C= NP_001052.3:p.His378=
NM_001130966.3:c.1132C= NP_001124438.2:p.His378=
NM_001166253.2:c.1270C= NP_001159725.2:p.His424=
NM_001166254.2:c.931C= NP_001159726.1:p.His311=
NM_001314028.2:c.1075C= NP_001300957.1:p.His359=
NM_001366537.1:c.949C= NP_001353466.1:p.His317=
NM_030984.4:c.1132C= NP_112246.3:p.His378=
XM_011516544.3:c.1135C= XP_011514846.1:p.His379=
XM_017012570.2:c.1135C= XP_016868059.1:p.His379=
XM_017012571.2:c.1135C= XP_016868060.1:p.His379=
XM_017012572.2:c.1135C= XP_016868061.1:p.His379=
XM_024446901.1:c.877C= XP_024302669.1:p.His293=
NM_001061.7:c.1132C= MANE Select NP_001052.3:p.His378=
NM_001130966.4:c.1132C= NP_001124438.2:p.His378=
NM_001166253.3:c.1270C= NP_001159725.2:p.His424=
NM_001166254.3:c.931C= NP_001159726.1:p.His311=
NM_001314028.3:c.1075C= NP_001300957.1:p.His359=
NM_001366537.2:c.949C= NP_001353466.1:p.His317=
NM_030984.5:c.1132C= NP_112246.3:p.His378=
NM_001130966.5:c.1132C= NP_001124438.2:p.His378=
NM_001166253.4:c.1270C= NP_001159725.2:p.His424=
NM_001166254.4:c.931C= NP_001159726.1:p.His311=
NM_001314028.4:c.1075C= NP_001300957.1:p.His359=
NM_001366537.3:c.949C= NP_001353466.1:p.His317=
NM_030984.6:c.1132C= NP_112246.3:p.His378=