Canonical Allele Identifier: CA352723658
Gene: QARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49104634G>C , CM000665.2:g.49104634G>C GRCh38
NC_000003.11:g.49142067G>C , CM000665.1:g.49142067G>C GRCh37
NC_000003.10:g.49117071G>C NCBI36
NG_042312.1:g.5496C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306125.12:c.100C>G MANE Select ENSP00000307567.6:p.Arg34Gly
ENST00000306125.11:c.100C>G ENSP00000307567.6:p.Arg34Gly
ENST00000414533.5:c.100C>G ENSP00000390015.1:p.Arg34Gly
ENST00000417025.2:n.126C>G
ENST00000418549.3:c.100C>G ENSP00000415247.1:p.Arg34Gly
ENST00000430182.5:c.100C>G ENSP00000389823.1:p.Arg34Gly
ENST00000452739.5:c.100C>G ENSP00000392850.2:p.Arg34Gly
ENST00000470619.6:n.119C>G
ENST00000479495.5:n.98-163C>G
ENST00000482261.7:n.176C>G
ENST00000482438.2:n.126C>G
ENST00000494767.2:c.100C>G ENSP00000489170.1:p.Arg34Gly
ENST00000634359.1:n.198-163C>G
ENST00000634527.1:c.-318-163C>G ENSP00000489039.1:n.-318-163C>G
ENST00000634602.1:c.100C>G ENSP00000489082.1:p.Arg34Gly
ENST00000634609.1:n.125C>G
ENST00000634724.1:n.124C>G
ENST00000634802.1:c.100C>G ENSP00000488917.1:p.Arg34Gly
ENST00000634953.1:n.127C>G
ENST00000635052.1:c.100C>G ENSP00000489409.1:p.Arg34Gly
ENST00000635194.1:c.100C>G ENSP00000488960.1:p.Arg34Gly
ENST00000635231.1:c.81+19C>G ENSP00000489550.1:n.81+19C>G
ENST00000635278.1:n.124C>G
ENST00000635443.1:c.100C>G ENSP00000489154.1:p.Arg34Gly
ENST00000635494.1:c.100C>G ENSP00000489331.1:p.Arg34Gly
ENST00000635501.1:n.490C>G
ENST00000635622.1:c.-364C>G ENSP00000489558.1:n.-364C>G
NM_001272073.1:c.100C>G NP_001259002.1:p.Arg34Gly
NM_005051.2:c.100C>G NP_005042.1:p.Arg34Gly
NR_073590.1:n.496C>G
XM_011533973.1:c.154C>G XP_011532275.1:p.Arg52Gly
XM_017006965.2:c.100C>G XP_016862454.2:p.Arg34Gly
NM_005051.3:c.100C>G MANE Select NP_005042.1:p.Arg34Gly
NM_001272073.2:c.100C>G NP_001259002.1:p.Arg34Gly
NR_073590.2:n.124C>G