Canonical Allele Identifier: CA1747340998

Gene: TBXAS1

Linked Data

• dbSNP Id: rs1810378859

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.139961908T>G , CM000669.2:g.139961908T>G	GRCh38
NC_000007.13:g.139661707T>G , CM000669.1:g.139661707T>G	GRCh37
NC_000007.12:g.139308176T>G	NCBI36
NG_008422.2:g.188527T>G , LRG_579:g.188527T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336425.10:c.820-11T>G	ENSP00000338087.7:n.820-11T>G
ENST00000411653.6:c.820-11T>G	ENSP00000411326.3:n.820-11T>G
ENST00000422328.6:c.*609-11T>G	ENSP00000415892.3:n.*609-11T>G
ENST00000448866.7:c.820-11T>G MANE Select	ENSP00000402536.3:n.820-11T>G
ENST00000458722.6:c.958-11T>G	ENSP00000411274.3:n.958-11T>G
ENST00000650822.1:c.823-11T>G	ENSP00000498517.1:n.823-11T>G
ENST00000652056.1:c.823-11T>G	ENSP00000498271.1:n.823-11T>G
ENST00000263552.10:c.823-11T>G	ENSP00000263552.6:n.823-11T>G
ENST00000336425.9:c.820-11T>G	ENSP00000338087.5:n.820-11T>G
ENST00000411653.5:c.820-11T>G	ENSP00000411326.1:n.820-11T>G
ENST00000414508.6:c.823-11T>G	ENSP00000392702.2:n.823-11T>G
ENST00000416849.6:c.961-11T>G	ENSP00000389414.2:n.961-11T>G
ENST00000422328.5:c.*609-11T>G	ENSP00000415892.1:n.*609-11T>G
ENST00000425687.5:c.619-11T>G	ENSP00000388736.1:n.619-11T>G
ENST00000448866.5:c.820-11T>G	ENSP00000402536.1:n.820-11T>G
ENST00000458722.5:c.958-11T>G	ENSP00000411274.1:n.958-11T>G
ENST00000462275.5:n.791-11T>G
ENST00000469630.1:n.303-11T>G
ENST00000494876.1:n.185-11T>G
NM_001061.4:c.823-11T>G	NP_001052.2:n.823-11T>G
NM_001130966.2:c.823-11T>G , LRG_579t1:c.823-11T>G	NP_001124438.1:n.823-11T>G
NM_001166253.1:c.961-11T>G , LRG_579t4:c.961-11T>G	NP_001159725.1:n.961-11T>G
NM_001166254.1:c.619-11T>G , LRG_579t3:c.619-11T>G	NP_001159726.1:n.619-11T>G
NM_001314028.1:c.763-11T>G	NP_001300957.1:n.763-11T>G
NM_030984.3:c.823-11T>G , LRG_579t2:c.823-11T>G	NP_112246.2:n.823-11T>G
NR_029394.1:c.-4294966209-11T>G
XM_011516544.1:c.823-11T>G	XP_011514846.1:n.823-11T>G
NM_001061.5:c.820-11T>G	NP_001052.3:n.820-11T>G
NM_001130966.3:c.820-11T>G	NP_001124438.2:n.820-11T>G
NM_001166253.2:c.958-11T>G	NP_001159725.2:n.958-11T>G
NM_001166254.2:c.619-11T>G	NP_001159726.1:n.619-11T>G
NM_001314028.2:c.763-11T>G	NP_001300957.1:n.763-11T>G
NM_001366537.1:c.637-11T>G	NP_001353466.1:n.637-11T>G
NM_030984.4:c.820-11T>G	NP_112246.3:n.820-11T>G
XM_011516544.3:c.823-11T>G	XP_011514846.1:n.823-11T>G
XM_017012570.2:c.823-11T>G	XP_016868059.1:n.823-11T>G
XM_017012571.2:c.823-11T>G	XP_016868060.1:n.823-11T>G
XM_017012572.2:c.823-11T>G	XP_016868061.1:n.823-11T>G
XM_024446901.1:c.565-11T>G	XP_024302669.1:n.565-11T>G
NM_001061.7:c.820-11T>G MANE Select	NP_001052.3:n.820-11T>G
NM_001130966.4:c.820-11T>G	NP_001124438.2:n.820-11T>G
NM_001166253.3:c.958-11T>G	NP_001159725.2:n.958-11T>G
NM_001166254.3:c.619-11T>G	NP_001159726.1:n.619-11T>G
NM_001314028.3:c.763-11T>G	NP_001300957.1:n.763-11T>G
NM_001366537.2:c.637-11T>G	NP_001353466.1:n.637-11T>G
NM_030984.5:c.820-11T>G	NP_112246.3:n.820-11T>G
NM_001130966.5:c.820-11T>G	NP_001124438.2:n.820-11T>G
NM_001166253.4:c.958-11T>G	NP_001159725.2:n.958-11T>G
NM_001166254.4:c.619-11T>G	NP_001159726.1:n.619-11T>G
NM_001314028.4:c.763-11T>G	NP_001300957.1:n.763-11T>G
NM_001366537.3:c.637-11T>G	NP_001353466.1:n.637-11T>G
NM_030984.6:c.820-11T>G	NP_112246.3:n.820-11T>G