Canonical Allele Identifier: CA433631323

Gene: QARS1

Linked Data

• MyVariant Identifiers: chr3:g.49142080C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49104647C>T , CM000665.2:g.49104647C>T	GRCh38
NC_000003.11:g.49142080C>T , CM000665.1:g.49142080C>T	GRCh37
NC_000003.10:g.49117084C>T	NCBI36
NG_042312.1:g.5483G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306125.12:c.87G>A MANE Select	ENSP00000307567.6:p.Leu29=
ENST00000306125.11:c.87G>A	ENSP00000307567.6:p.Leu29=
ENST00000414533.5:c.87G>A	ENSP00000390015.1:p.Leu29=
ENST00000417025.2:n.113G>A
ENST00000418549.3:c.87G>A	ENSP00000415247.1:p.Leu29=
ENST00000430182.5:c.87G>A	ENSP00000389823.1:p.Leu29=
ENST00000452739.5:c.87G>A	ENSP00000392850.2:p.Leu29=
ENST00000470619.6:n.106G>A
ENST00000479495.5:n.98-176G>A
ENST00000482261.7:n.163G>A
ENST00000482438.2:n.113G>A
ENST00000494767.2:c.87G>A	ENSP00000489170.1:p.Leu29=
ENST00000634359.1:n.198-176G>A
ENST00000634527.1:c.-318-176G>A	ENSP00000489039.1:n.-318-176G>A
ENST00000634602.1:c.87G>A	ENSP00000489082.1:p.Leu29=
ENST00000634609.1:n.112G>A
ENST00000634724.1:n.111G>A
ENST00000634802.1:c.87G>A	ENSP00000488917.1:p.Leu29=
ENST00000634953.1:n.114G>A
ENST00000635052.1:c.87G>A	ENSP00000489409.1:p.Leu29=
ENST00000635194.1:c.87G>A	ENSP00000488960.1:p.Leu29=
ENST00000635231.1:c.81+6G>A	ENSP00000489550.1:n.81+6G>A
ENST00000635278.1:n.111G>A
ENST00000635443.1:c.87G>A	ENSP00000489154.1:p.Leu29=
ENST00000635494.1:c.87G>A	ENSP00000489331.1:p.Leu29=
ENST00000635501.1:n.477G>A
ENST00000635622.1:c.-377G>A	ENSP00000489558.1:n.-377G>A
NM_001272073.1:c.87G>A	NP_001259002.1:p.Leu29=
NM_005051.2:c.87G>A	NP_005042.1:p.Leu29=
NR_073590.1:n.483G>A
XM_011533973.1:c.141G>A	XP_011532275.1:p.Leu47=
XM_017006965.2:c.87G>A	XP_016862454.2:p.Leu29=
NM_005051.3:c.87G>A MANE Select	NP_005042.1:p.Leu29=
NM_001272073.2:c.87G>A	NP_001259002.1:p.Leu29=
NR_073590.2:n.111G>A