Canonical Allele Identifier: CA352723622

Gene: QARS1

Linked Data

• gnomAD v4: 3-49104625-C-A
• MyVariant Identifiers: chr3:g.49142058C>A (hg19) ; chr3:g.49104625C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49104625C>A , CM000665.2:g.49104625C>A	GRCh38
NC_000003.11:g.49142058C>A , CM000665.1:g.49142058C>A	GRCh37
NC_000003.10:g.49117062C>A	NCBI36
NG_042312.1:g.5505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306125.12:c.109G>T MANE Select	ENSP00000307567.6:p.Ala37Ser
ENST00000306125.11:c.109G>T	ENSP00000307567.6:p.Ala37Ser
ENST00000414533.5:c.109G>T	ENSP00000390015.1:p.Ala37Ser
ENST00000417025.2:n.135G>T
ENST00000418549.3:c.109G>T	ENSP00000415247.1:p.Ala37Ser
ENST00000430182.5:c.109G>T	ENSP00000389823.1:p.Ala37Ser
ENST00000452739.5:c.109G>T	ENSP00000392850.2:p.Ala37Ser
ENST00000470619.6:n.128G>T
ENST00000479495.5:n.98-154G>T
ENST00000482261.7:n.185G>T
ENST00000482438.2:n.135G>T
ENST00000494767.2:c.109G>T	ENSP00000489170.1:p.Ala37Ser
ENST00000634359.1:n.198-154G>T
ENST00000634527.1:c.-318-154G>T	ENSP00000489039.1:n.-318-154G>T
ENST00000634602.1:c.109G>T	ENSP00000489082.1:p.Ala37Ser
ENST00000634609.1:n.134G>T
ENST00000634724.1:n.133G>T
ENST00000634802.1:c.109G>T	ENSP00000488917.1:p.Ala37Ser
ENST00000634953.1:n.136G>T
ENST00000635052.1:c.109G>T	ENSP00000489409.1:p.Ala37Ser
ENST00000635194.1:c.109G>T	ENSP00000488960.1:p.Ala37Ser
ENST00000635231.1:c.81+28G>T	ENSP00000489550.1:n.81+28G>T
ENST00000635278.1:n.133G>T
ENST00000635443.1:c.109G>T	ENSP00000489154.1:p.Ala37Ser
ENST00000635494.1:c.109G>T	ENSP00000489331.1:p.Ala37Ser
ENST00000635501.1:n.499G>T
ENST00000635622.1:c.-355G>T	ENSP00000489558.1:n.-355G>T
NM_001272073.1:c.109G>T	NP_001259002.1:p.Ala37Ser
NM_005051.2:c.109G>T	NP_005042.1:p.Ala37Ser
NR_073590.1:n.505G>T
XM_011533973.1:c.163G>T	XP_011532275.1:p.Ala55Ser
XM_017006965.2:c.109G>T	XP_016862454.2:p.Ala37Ser
NM_005051.3:c.109G>T MANE Select	NP_005042.1:p.Ala37Ser
NM_001272073.2:c.109G>T	NP_001259002.1:p.Ala37Ser
NR_073590.2:n.133G>T