Canonical Allele Identifier: CA1624924422

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303375C= , CM000668.2:g.44303375C= GRCh38
NC_000006.11:g.44271112C= , CM000668.1:g.44271112C= GRCh37
NC_000006.10:g.44379090C= NCBI36
NG_031952.1:g.14952G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.2056G= (AARS2) MANE Select ENSP00000244571.4:p.Glu686=
ENST00000244571.4:c.2056G= (AARS2) ENSP00000244571.4:p.Glu686=
ENST00000438774.2:c.577-3568C= (TMEM151B) ENSP00000409337.2:n.577-3568C=
ENST00000505802.1:c.314-3568C=
NM_020745.3:c.2056G= (AARS2) NP_065796.1:p.Glu686=
XM_005249245.2:c.1765G= (AARS2) XP_005249302.1:p.Glu589=
XM_011514764.1:c.2056G= (AARS2) XP_011513066.1:p.Glu686=
XR_241907.2:n.2091G= (AARS2)
XM_005249245.3:c.1765G= (AARS2) XP_005249302.1:p.Glu589=
XM_011514764.2:c.2056G= (AARS2) XP_011513066.1:p.Glu686=
XM_017011112.1:c.766G= (AARS2) XP_016866601.1:p.Glu256=
NM_020745.4:c.2056G= (AARS2) MANE Select NP_065796.2:p.Glu686=
NM_001318876.2:c.946-138515C= (POLR1C) NP_001305805.1:n.946-138515C=