Canonical Allele Identifier: CA369519549

Gene: TBXAS1

Linked Data

• MyVariant Identifiers: chr7:g.139717478G>A (hg19) ; chr7:g.140017678G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140017678G>A , CM000669.2:g.140017678G>A	GRCh38
NC_000007.13:g.139717478G>A , CM000669.1:g.139717478G>A	GRCh37
NC_000007.12:g.139363947G>A	NCBI36
NG_008422.2:g.244297G>A , LRG_579:g.244297G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336425.10:c.1372G>A	ENSP00000338087.7:p.Ala458Thr
ENST00000411653.6:c.1364+1818G>A	ENSP00000411326.3:n.1364+1818G>A
ENST00000422328.6:c.*1161G>A	ENSP00000415892.3:n.*1161G>A
ENST00000448866.7:c.1372G>A MANE Select	ENSP00000402536.3:p.Ala458Thr
ENST00000458722.6:c.1510G>A	ENSP00000411274.3:p.Ala504Thr
ENST00000650822.1:c.1375G>A	ENSP00000498517.1:p.Ala459Thr
ENST00000652056.1:c.1367+1818G>A	ENSP00000498271.1:n.1367+1818G>A
ENST00000263552.10:c.1375G>A	ENSP00000263552.6:p.Ala459Thr
ENST00000336425.9:c.1372G>A	ENSP00000338087.5:p.Ala458Thr
ENST00000411653.5:c.1364+1818G>A	ENSP00000411326.1:n.1364+1818G>A
ENST00000414508.6:c.1367+1818G>A	ENSP00000392702.2:n.1367+1818G>A
ENST00000416849.6:c.1513G>A	ENSP00000389414.2:p.Ala505Thr
ENST00000422328.5:c.*1161G>A	ENSP00000415892.1:n.*1161G>A
ENST00000425687.5:c.1171G>A	ENSP00000388736.1:p.Ala391Thr
ENST00000448866.5:c.1372G>A	ENSP00000402536.1:p.Ala458Thr
ENST00000458722.5:c.1510G>A	ENSP00000411274.1:p.Ala504Thr
NM_001061.4:c.1375G>A	NP_001052.2:p.Ala459Thr
NM_001130966.2:c.1375G>A , LRG_579t1:c.1375G>A	NP_001124438.1:p.Ala459Thr
NM_001166253.1:c.1513G>A , LRG_579t4:c.1513G>A	NP_001159725.1:p.Ala505Thr
NM_001166254.1:c.1171G>A , LRG_579t3:c.1171G>A	NP_001159726.1:p.Ala391Thr
NM_001314028.1:c.1315G>A	NP_001300957.1:p.Ala439Thr
NM_030984.3:c.1367+1818G>A , LRG_579t2:c.1367+1818G>A	NP_112246.2:n.1367+1818G>A
NR_029394.1:c.-4294965657G>A
NM_001061.5:c.1372G>A	NP_001052.3:p.Ala458Thr
NM_001130966.3:c.1372G>A	NP_001124438.2:p.Ala458Thr
NM_001166253.2:c.1510G>A	NP_001159725.2:p.Ala504Thr
NM_001166254.2:c.1171G>A	NP_001159726.1:p.Ala391Thr
NM_001314028.2:c.1315G>A	NP_001300957.1:p.Ala439Thr
NM_001366537.1:c.1189G>A	NP_001353466.1:p.Ala397Thr
NM_030984.4:c.1364+1818G>A	NP_112246.3:n.1364+1818G>A
XM_024446901.1:c.1117G>A	XP_024302669.1:p.Ala373Thr
NM_001061.7:c.1372G>A MANE Select	NP_001052.3:p.Ala458Thr
NM_001130966.4:c.1372G>A	NP_001124438.2:p.Ala458Thr
NM_001166253.3:c.1510G>A	NP_001159725.2:p.Ala504Thr
NM_001166254.3:c.1171G>A	NP_001159726.1:p.Ala391Thr
NM_001314028.3:c.1315G>A	NP_001300957.1:p.Ala439Thr
NM_001366537.2:c.1189G>A	NP_001353466.1:p.Ala397Thr
NM_030984.5:c.1364+1818G>A	NP_112246.3:n.1364+1818G>A
NM_001130966.5:c.1372G>A	NP_001124438.2:p.Ala458Thr
NM_001166253.4:c.1510G>A	NP_001159725.2:p.Ala504Thr
NM_001166254.4:c.1171G>A	NP_001159726.1:p.Ala391Thr
NM_001314028.4:c.1315G>A	NP_001300957.1:p.Ala439Thr
NM_001366537.3:c.1189G>A	NP_001353466.1:p.Ala397Thr
NM_030984.6:c.1364+1818G>A	NP_112246.3:n.1364+1818G>A