Canonical Allele Identifier: CA382176991

Gene: NARS2

Linked Data

• MyVariant Identifiers: chr11:g.78189651A>T (hg19) ; chr11:g.78478605A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478605A>T , CM000673.2:g.78478605A>T	GRCh38
NC_000011.9:g.78189651A>T , CM000673.1:g.78189651A>T	GRCh37
NC_000011.8:g.77867299A>T	NCBI36
NG_042046.1:g.101260T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.391T>A
ENST00000529771.2:c.220T>A	ENSP00000435298.2:p.Phe74Ile
ENST00000695114.1:n.3562T>A
ENST00000695115.1:c.220T>A	ENSP00000511705.1:p.Phe74Ile
ENST00000695116.1:c.142-9292T>A	ENSP00000511706.1:n.142-9292T>A
ENST00000695341.1:c.*571T>A	ENSP00000511816.1:n.*571T>A
ENST00000695342.1:c.220T>A	ENSP00000511817.1:p.Phe74Ile
ENST00000695343.1:c.220T>A	ENSP00000511818.1:p.Phe74Ile
ENST00000695344.1:c.820T>A	ENSP00000511819.1:p.Phe274Ile
ENST00000695345.1:c.220T>A	ENSP00000511820.1:p.Phe74Ile
ENST00000695346.1:c.*318T>A	ENSP00000511821.1:n.*318T>A
ENST00000695347.1:c.*373T>A	ENSP00000511822.1:n.*373T>A
ENST00000695348.1:c.220T>A	ENSP00000511823.1:p.Phe74Ile
ENST00000695349.1:c.901T>A	ENSP00000511824.1:p.Phe301Ile
ENST00000695350.1:c.*72T>A	ENSP00000511825.1:n.*72T>A
ENST00000695351.1:c.823-12592T>A	ENSP00000511826.1:n.823-12592T>A
ENST00000695352.1:c.49T>A	ENSP00000511827.1:p.Phe17Ile
ENST00000695353.1:c.-105-12592T>A	ENSP00000511828.1:n.-105-12592T>A
ENST00000695354.1:c.901T>A	ENSP00000511829.1:p.Phe301Ile
ENST00000695355.1:c.901T>A	ENSP00000511830.1:p.Phe301Ile
ENST00000695356.1:c.*882T>A	ENSP00000511831.1:n.*882T>A
ENST00000695357.1:c.901T>A	ENSP00000511832.1:p.Phe301Ile
ENST00000695358.1:c.901T>A	ENSP00000511833.1:p.Phe301Ile
ENST00000695359.1:c.*558T>A	ENSP00000511834.1:n.*558T>A
ENST00000695360.1:c.901T>A	ENSP00000511835.1:p.Phe301Ile
ENST00000695361.1:c.*89-9292T>A	ENSP00000511836.1:n.*89-9292T>A
ENST00000695362.1:c.*221T>A	ENSP00000511837.1:n.*221T>A
ENST00000695364.1:n.1239T>A
ENST00000695365.1:n.1191T>A
ENST00000695366.1:c.901T>A	ENSP00000511838.1:p.Phe301Ile
ENST00000281038.10:c.901T>A MANE Select	ENSP00000281038.5:p.Phe301Ile
ENST00000281038.9:c.901T>A	ENSP00000281038.5:p.Phe301Ile
ENST00000525345.5:c.391T>A
ENST00000528850.5:c.220T>A	ENSP00000432635.1:p.Phe74Ile
ENST00000529880.1:c.595-12592T>A	ENSP00000432240.1:n.595-12592T>A
NM_001243251.1:c.220T>A	NP_001230180.1:p.Phe74Ile
NM_024678.5:c.901T>A	NP_078954.4:p.Phe301Ile
XM_011545253.1:c.901T>A	XP_011543555.1:p.Phe301Ile
XR_950050.1:n.1270T>A
XR_950051.1:n.1270T>A
XR_950344.1:n.199+3728A>T
XR_950345.1:n.151+5309A>T
XM_011545253.2:c.901T>A	XP_011543555.1:p.Phe301Ile
XM_017018302.2:c.901T>A	XP_016873791.1:p.Phe301Ile
XM_017018303.1:c.220T>A	XP_016873792.1:p.Phe74Ile
XM_017018304.2:c.220T>A	XP_016873793.1:p.Phe74Ile
XR_001747963.2:n.1255T>A
XR_001747964.2:n.1255T>A
XR_001747965.2:n.1255T>A
XR_001747966.2:n.1255T>A
XR_001748314.1:n.3035+3728A>T
NM_024678.6:c.901T>A MANE Select	NP_078954.4:p.Phe301Ile
NM_001243251.2:c.220T>A	NP_001230180.1:p.Phe74Ile