Canonical Allele Identifier: CA1363328737
Gene: QARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49104652C= , CM000665.2:g.49104652C= GRCh38
NC_000003.11:g.49142085C= , CM000665.1:g.49142085C= GRCh37
NC_000003.10:g.49117089C= NCBI36
NG_042312.1:g.5478G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306125.12:c.82G= MANE Select ENSP00000307567.6:p.Ala28=
ENST00000306125.11:c.82G= ENSP00000307567.6:p.Ala28=
ENST00000414533.5:c.82G= ENSP00000390015.1:p.Ala28=
ENST00000417025.2:n.108G=
ENST00000418549.3:c.82G= ENSP00000415247.1:p.Ala28=
ENST00000430182.5:c.82G= ENSP00000389823.1:p.Ala28=
ENST00000452739.5:c.82G= ENSP00000392850.2:p.Ala28=
ENST00000470619.6:n.101G=
ENST00000479495.5:n.98-181G=
ENST00000482261.7:n.158G=
ENST00000482438.2:n.108G=
ENST00000494767.2:c.82G= ENSP00000489170.1:p.Ala28=
ENST00000634359.1:n.198-181G=
ENST00000634527.1:c.-318-181G= ENSP00000489039.1:n.-318-181G=
ENST00000634602.1:c.82G= ENSP00000489082.1:p.Ala28=
ENST00000634609.1:n.107G=
ENST00000634724.1:n.106G=
ENST00000634802.1:c.82G= ENSP00000488917.1:p.Ala28=
ENST00000634953.1:n.109G=
ENST00000635052.1:c.82G= ENSP00000489409.1:p.Ala28=
ENST00000635194.1:c.82G= ENSP00000488960.1:p.Ala28=
ENST00000635231.1:c.81+1G= ENSP00000489550.1:n.81+1G=
ENST00000635278.1:n.106G=
ENST00000635443.1:c.82G= ENSP00000489154.1:p.Ala28=
ENST00000635494.1:c.82G= ENSP00000489331.1:p.Ala28=
ENST00000635501.1:n.472G=
ENST00000635622.1:c.-382G= ENSP00000489558.1:n.-382G=
NM_001272073.1:c.82G= NP_001259002.1:p.Ala28=
NM_005051.2:c.82G= NP_005042.1:p.Ala28=
NR_073590.1:n.478G=
XM_011533973.1:c.136G= XP_011532275.1:p.Ala46=
XM_017006965.2:c.82G= XP_016862454.2:p.Ala28=
NM_005051.3:c.82G= MANE Select NP_005042.1:p.Ala28=
NM_001272073.2:c.82G= NP_001259002.1:p.Ala28=
NR_073590.2:n.106G=