Canonical Allele Identifier: CA369584409

Gene: TBXAS1

Linked Data

• MyVariant Identifiers: chr7:g.139661800G>C (hg19) ; chr7:g.139962001G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.139962001G>C , CM000669.2:g.139962001G>C	GRCh38
NC_000007.13:g.139661800G>C , CM000669.1:g.139661800G>C	GRCh37
NC_000007.12:g.139308269G>C	NCBI36
NG_008422.2:g.188620G>C , LRG_579:g.188620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336425.10:c.902G>C	ENSP00000338087.7:p.Arg301Thr
ENST00000411653.6:c.902G>C	ENSP00000411326.3:p.Arg301Thr
ENST00000422328.6:c.*691G>C	ENSP00000415892.3:n.*691G>C
ENST00000448866.7:c.902G>C MANE Select	ENSP00000402536.3:p.Arg301Thr
ENST00000458722.6:c.1040G>C	ENSP00000411274.3:p.Arg347Thr
ENST00000650822.1:c.905G>C	ENSP00000498517.1:p.Arg302Thr
ENST00000652056.1:c.905G>C	ENSP00000498271.1:p.Arg302Thr
ENST00000263552.10:c.905G>C	ENSP00000263552.6:p.Arg302Thr
ENST00000336425.9:c.902G>C	ENSP00000338087.5:p.Arg301Thr
ENST00000411653.5:c.902G>C	ENSP00000411326.1:p.Arg301Thr
ENST00000414508.6:c.905G>C	ENSP00000392702.2:p.Arg302Thr
ENST00000416849.6:c.1043G>C	ENSP00000389414.2:p.Arg348Thr
ENST00000422328.5:c.*691G>C	ENSP00000415892.1:n.*691G>C
ENST00000425687.5:c.701G>C	ENSP00000388736.1:p.Arg234Thr
ENST00000448866.5:c.902G>C	ENSP00000402536.1:p.Arg301Thr
ENST00000458722.5:c.1040G>C	ENSP00000411274.1:p.Arg347Thr
ENST00000462275.5:n.873G>C
ENST00000469630.1:n.385G>C
ENST00000494876.1:n.267G>C
NM_001061.4:c.905G>C	NP_001052.2:p.Arg302Thr
NM_001130966.2:c.905G>C , LRG_579t1:c.905G>C	NP_001124438.1:p.Arg302Thr
NM_001166253.1:c.1043G>C , LRG_579t4:c.1043G>C	NP_001159725.1:p.Arg348Thr
NM_001166254.1:c.701G>C , LRG_579t3:c.701G>C	NP_001159726.1:p.Arg234Thr
NM_001314028.1:c.845G>C	NP_001300957.1:p.Arg282Thr
NM_030984.3:c.905G>C , LRG_579t2:c.905G>C	NP_112246.2:p.Arg302Thr
NR_029394.1:c.-4294966127G>C
XM_011516544.1:c.905G>C	XP_011514846.1:p.Arg302Thr
NM_001061.5:c.902G>C	NP_001052.3:p.Arg301Thr
NM_001130966.3:c.902G>C	NP_001124438.2:p.Arg301Thr
NM_001166253.2:c.1040G>C	NP_001159725.2:p.Arg347Thr
NM_001166254.2:c.701G>C	NP_001159726.1:p.Arg234Thr
NM_001314028.2:c.845G>C	NP_001300957.1:p.Arg282Thr
NM_001366537.1:c.719G>C	NP_001353466.1:p.Arg240Thr
NM_030984.4:c.902G>C	NP_112246.3:p.Arg301Thr
XM_011516544.3:c.905G>C	XP_011514846.1:p.Arg302Thr
XM_017012570.2:c.905G>C	XP_016868059.1:p.Arg302Thr
XM_017012571.2:c.905G>C	XP_016868060.1:p.Arg302Thr
XM_017012572.2:c.905G>C	XP_016868061.1:p.Arg302Thr
XM_024446901.1:c.647G>C	XP_024302669.1:p.Arg216Thr
NM_001061.7:c.902G>C MANE Select	NP_001052.3:p.Arg301Thr
NM_001130966.4:c.902G>C	NP_001124438.2:p.Arg301Thr
NM_001166253.3:c.1040G>C	NP_001159725.2:p.Arg347Thr
NM_001166254.3:c.701G>C	NP_001159726.1:p.Arg234Thr
NM_001314028.3:c.845G>C	NP_001300957.1:p.Arg282Thr
NM_001366537.2:c.719G>C	NP_001353466.1:p.Arg240Thr
NM_030984.5:c.902G>C	NP_112246.3:p.Arg301Thr
NM_001130966.5:c.902G>C	NP_001124438.2:p.Arg301Thr
NM_001166253.4:c.1040G>C	NP_001159725.2:p.Arg347Thr
NM_001166254.4:c.701G>C	NP_001159726.1:p.Arg234Thr
NM_001314028.4:c.845G>C	NP_001300957.1:p.Arg282Thr
NM_001366537.3:c.719G>C	NP_001353466.1:p.Arg240Thr
NM_030984.6:c.902G>C	NP_112246.3:p.Arg301Thr