Canonical Allele Identifier: CA1747318428
Gene: TBXAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.139911239G= , CM000669.2:g.139911239G= GRCh38
NC_000007.13:g.139611038G= , CM000669.1:g.139611038G= GRCh37
NC_000007.12:g.139257507G= NCBI36
NG_008422.2:g.137858G= , LRG_579:g.137858G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336425.10:c.251G= ENSP00000338087.7:p.Arg84=
ENST00000411653.6:c.251G= ENSP00000411326.3:p.Arg84=
ENST00000414041.2:c.*106G= ENSP00000412710.3:n.*106G=
ENST00000422328.6:c.*40G= ENSP00000415892.3:n.*40G=
ENST00000438104.6:c.251G= ENSP00000388612.3:p.Arg84=
ENST00000448866.7:c.251G= MANE Select ENSP00000402536.3:p.Arg84=
ENST00000455353.6:c.251G= ENSP00000391567.3:p.Arg84=
ENST00000458722.6:c.251G= ENSP00000411274.3:p.Arg84=
ENST00000650822.1:c.254G= ENSP00000498517.1:p.Arg85=
ENST00000652056.1:c.254G= ENSP00000498271.1:p.Arg85=
ENST00000263552.10:c.254G= ENSP00000263552.6:p.Arg85=
ENST00000336425.9:c.251G= ENSP00000338087.5:p.Arg84=
ENST00000411653.5:c.251G= ENSP00000411326.1:p.Arg84=
ENST00000414041.1:c.*106G= ENSP00000412710.1:n.*106G=
ENST00000414508.6:c.254G= ENSP00000392702.2:p.Arg85=
ENST00000416849.6:c.254G= ENSP00000389414.2:p.Arg85=
ENST00000422328.5:c.*40G= ENSP00000415892.1:n.*40G=
ENST00000425687.5:c.50G= ENSP00000388736.1:p.Arg17=
ENST00000438104.5:c.251G= ENSP00000388612.1:p.Arg84=
ENST00000448866.5:c.251G= ENSP00000402536.1:p.Arg84=
ENST00000455353.5:c.251G= ENSP00000391567.1:p.Arg84=
ENST00000458722.5:c.251G= ENSP00000411274.1:p.Arg84=
ENST00000462275.5:n.222G=
ENST00000476637.5:n.357-24952G=
NM_001061.4:c.254G= NP_001052.2:p.Arg85=
NM_001130966.2:c.254G= , LRG_579t1:c.254G= NP_001124438.1:p.Arg85=
NM_001166253.1:c.254G= , LRG_579t4:c.254G= NP_001159725.1:p.Arg85=
NM_001166254.1:c.50G= , LRG_579t3:c.50G= NP_001159726.1:p.Arg17=
NM_001314028.1:c.194G= NP_001300957.1:p.Arg65=
NM_030984.3:c.254G= , LRG_579t2:c.254G= NP_112246.2:p.Arg85=
NR_029394.1:c.-4294966778G=
XM_011516544.1:c.254G= XP_011514846.1:p.Arg85=
NM_001061.5:c.251G= NP_001052.3:p.Arg84=
NM_001130966.3:c.251G= NP_001124438.2:p.Arg84=
NM_001166253.2:c.251G= NP_001159725.2:p.Arg84=
NM_001166254.2:c.50G= NP_001159726.1:p.Arg17=
NM_001314028.2:c.194G= NP_001300957.1:p.Arg65=
NM_001366537.1:c.151-24952G= NP_001353466.1:n.151-24952G=
NM_001366538.1:c.251G= NP_001353467.1:p.Arg84=
NM_030984.4:c.251G= NP_112246.3:p.Arg84=
XM_011516544.3:c.254G= XP_011514846.1:p.Arg85=
XM_017012570.2:c.254G= XP_016868059.1:p.Arg85=
XM_017012571.2:c.254G= XP_016868060.1:p.Arg85=
XM_017012572.2:c.254G= XP_016868061.1:p.Arg85=
XM_024446901.1:c.-5G= XP_024302669.1:n.-5G=
NM_001061.7:c.251G= MANE Select NP_001052.3:p.Arg84=
NM_001130966.4:c.251G= NP_001124438.2:p.Arg84=
NM_001166253.3:c.251G= NP_001159725.2:p.Arg84=
NM_001166254.3:c.50G= NP_001159726.1:p.Arg17=
NM_001314028.3:c.194G= NP_001300957.1:p.Arg65=
NM_001366537.2:c.151-24952G= NP_001353466.1:n.151-24952G=
NM_001366538.2:c.251G= NP_001353467.1:p.Arg84=
NM_030984.5:c.251G= NP_112246.3:p.Arg84=
NM_001130966.5:c.251G= NP_001124438.2:p.Arg84=
NM_001166253.4:c.251G= NP_001159725.2:p.Arg84=
NM_001166254.4:c.50G= NP_001159726.1:p.Arg17=
NM_001314028.4:c.194G= NP_001300957.1:p.Arg65=
NM_001366537.3:c.151-24952G= NP_001353466.1:n.151-24952G=
NM_030984.6:c.251G= NP_112246.3:p.Arg84=