Canonical Allele Identifier: CA476050108

Gene: NARS2

Linked Data

• MyVariant Identifiers: chr11:g.78189703T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478657T>C , CM000673.2:g.78478657T>C	GRCh38
NC_000011.9:g.78189703T>C , CM000673.1:g.78189703T>C	GRCh37
NC_000011.8:g.77867351T>C	NCBI36
NG_042046.1:g.101208A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.339A>G
ENST00000529771.2:c.168A>G	ENSP00000435298.2:p.Thr56=
ENST00000695114.1:n.3510A>G
ENST00000695115.1:c.168A>G	ENSP00000511705.1:p.Thr56=
ENST00000695116.1:c.142-9344A>G	ENSP00000511706.1:n.142-9344A>G
ENST00000695341.1:c.*519A>G	ENSP00000511816.1:n.*519A>G
ENST00000695342.1:c.168A>G	ENSP00000511817.1:p.Thr56=
ENST00000695343.1:c.168A>G	ENSP00000511818.1:p.Thr56=
ENST00000695344.1:c.768A>G	ENSP00000511819.1:p.Thr256=
ENST00000695345.1:c.168A>G	ENSP00000511820.1:p.Thr56=
ENST00000695346.1:c.*266A>G	ENSP00000511821.1:n.*266A>G
ENST00000695347.1:c.*321A>G	ENSP00000511822.1:n.*321A>G
ENST00000695348.1:c.168A>G	ENSP00000511823.1:p.Thr56=
ENST00000695349.1:c.849A>G	ENSP00000511824.1:p.Thr283=
ENST00000695350.1:c.*20A>G	ENSP00000511825.1:n.*20A>G
ENST00000695351.1:c.823-12644A>G	ENSP00000511826.1:n.823-12644A>G
ENST00000695352.1:c.-4A>G	ENSP00000511827.1:n.-4A>G
ENST00000695353.1:c.-105-12644A>G	ENSP00000511828.1:n.-105-12644A>G
ENST00000695354.1:c.849A>G	ENSP00000511829.1:p.Thr283=
ENST00000695355.1:c.849A>G	ENSP00000511830.1:p.Thr283=
ENST00000695356.1:c.*830A>G	ENSP00000511831.1:n.*830A>G
ENST00000695357.1:c.849A>G	ENSP00000511832.1:p.Thr283=
ENST00000695358.1:c.849A>G	ENSP00000511833.1:p.Thr283=
ENST00000695359.1:c.*506A>G	ENSP00000511834.1:n.*506A>G
ENST00000695360.1:c.849A>G	ENSP00000511835.1:p.Thr283=
ENST00000695361.1:c.*89-9344A>G	ENSP00000511836.1:n.*89-9344A>G
ENST00000695362.1:c.*169A>G	ENSP00000511837.1:n.*169A>G
ENST00000695364.1:n.1187A>G
ENST00000695365.1:n.1139A>G
ENST00000695366.1:c.849A>G	ENSP00000511838.1:p.Thr283=
ENST00000281038.10:c.849A>G MANE Select	ENSP00000281038.5:p.Thr283=
ENST00000281038.9:c.849A>G	ENSP00000281038.5:p.Thr283=
ENST00000525345.5:c.339A>G
ENST00000528850.5:c.168A>G	ENSP00000432635.1:p.Thr56=
ENST00000529880.1:c.595-12644A>G	ENSP00000432240.1:n.595-12644A>G
NM_001243251.1:c.168A>G	NP_001230180.1:p.Thr56=
NM_024678.5:c.849A>G	NP_078954.4:p.Thr283=
XM_011545253.1:c.849A>G	XP_011543555.1:p.Thr283=
XR_950050.1:n.1218A>G
XR_950051.1:n.1218A>G
XR_950344.1:n.199+3780T>C
XR_950345.1:n.151+5361T>C
XM_011545253.2:c.849A>G	XP_011543555.1:p.Thr283=
XM_017018302.2:c.849A>G	XP_016873791.1:p.Thr283=
XM_017018303.1:c.168A>G	XP_016873792.1:p.Thr56=
XM_017018304.2:c.168A>G	XP_016873793.1:p.Thr56=
XR_001747963.2:n.1203A>G
XR_001747964.2:n.1203A>G
XR_001747965.2:n.1203A>G
XR_001747966.2:n.1203A>G
XR_001748314.1:n.3035+3780T>C
NM_024678.6:c.849A>G MANE Select	NP_078954.4:p.Thr283=
NM_001243251.2:c.168A>G	NP_001230180.1:p.Thr56=