Canonical Allele Identifier: CA476052083

Gene: NARS2

Linked Data

• MyVariant Identifiers: chr11:g.78285417C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78574372C>T , CM000673.2:g.78574372C>T	GRCh38
NC_000011.9:g.78285417C>T , CM000673.1:g.78285417C>T	GRCh37
NC_000011.8:g.77963065C>T	NCBI36
NG_042046.1:g.5493G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529771.2:c.-541+457G>A	ENSP00000435298.2:n.-541+457G>A
ENST00000695114.1:n.419G>A
ENST00000695115.1:c.-633+457G>A	ENSP00000511705.1:n.-633+457G>A
ENST00000695116.1:c.-541+457G>A	ENSP00000511706.1:n.-541+457G>A
ENST00000695117.1:n.36+457G>A
ENST00000695341.1:c.117G>A	ENSP00000511816.1:p.Ala39=
ENST00000695342.1:c.-541+418G>A	ENSP00000511817.1:n.-541+418G>A
ENST00000695343.1:c.-804+457G>A	ENSP00000511818.1:n.-804+457G>A
ENST00000695344.1:c.117G>A	ENSP00000511819.1:p.Ala39=
ENST00000695345.1:c.-541+457G>A	ENSP00000511820.1:n.-541+457G>A
ENST00000695346.1:c.117G>A	ENSP00000511821.1:p.Ala39=
ENST00000695347.1:c.117G>A	ENSP00000511822.1:p.Ala39=
ENST00000695348.1:c.-460+457G>A	ENSP00000511823.1:n.-460+457G>A
ENST00000695349.1:c.117G>A	ENSP00000511824.1:p.Ala39=
ENST00000695350.1:c.117G>A	ENSP00000511825.1:p.Ala39=
ENST00000695351.1:c.117G>A	ENSP00000511826.1:p.Ala39=
ENST00000695352.1:c.-579+457G>A	ENSP00000511827.1:n.-579+457G>A
ENST00000695353.1:c.-654+457G>A	ENSP00000511828.1:n.-654+457G>A
ENST00000695354.1:c.117G>A	ENSP00000511829.1:p.Ala39=
ENST00000695355.1:c.117G>A	ENSP00000511830.1:p.Ala39=
ENST00000695356.1:c.117G>A	ENSP00000511831.1:p.Ala39=
ENST00000695357.1:c.117G>A	ENSP00000511832.1:p.Ala39=
ENST00000695358.1:c.117G>A	ENSP00000511833.1:p.Ala39=
ENST00000695359.1:c.117G>A	ENSP00000511834.1:p.Ala39=
ENST00000695360.1:c.117G>A	ENSP00000511835.1:p.Ala39=
ENST00000695361.1:c.117G>A	ENSP00000511836.1:p.Ala39=
ENST00000695362.1:c.117G>A	ENSP00000511837.1:p.Ala39=
ENST00000695364.1:n.455G>A
ENST00000695365.1:n.407G>A
ENST00000695366.1:c.117G>A	ENSP00000511838.1:p.Ala39=
ENST00000281038.10:c.117G>A MANE Select	ENSP00000281038.5:p.Ala39=
ENST00000281038.9:c.117G>A	ENSP00000281038.5:p.Ala39=
ENST00000529571.1:c.-541+457G>A	ENSP00000433478.1:n.-541+457G>A
ENST00000529880.1:c.117G>A	ENSP00000432240.1:p.Ala39=
NM_001243251.1:c.-541+457G>A	NP_001230180.1:n.-541+457G>A
NM_024678.5:c.117G>A	NP_078954.4:p.Ala39=
XM_011545253.1:c.117G>A	XP_011543555.1:p.Ala39=
XR_950050.1:n.486G>A
XR_950051.1:n.486G>A
XM_011545253.2:c.117G>A	XP_011543555.1:p.Ala39=
XM_017018302.2:c.117G>A	XP_016873791.1:p.Ala39=
XM_017018303.1:c.-613+457G>A	XP_016873792.1:n.-613+457G>A
XM_017018304.2:c.-541+457G>A	XP_016873793.1:n.-541+457G>A
XR_001747963.2:n.471G>A
XR_001747964.2:n.471G>A
XR_001747965.2:n.471G>A
XR_001747966.2:n.471G>A
NM_024678.6:c.117G>A MANE Select	NP_078954.4:p.Ala39=
NM_001243251.2:c.-541+457G>A	NP_001230180.1:n.-541+457G>A