Canonical Allele Identifier: CA1624922852

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302065C= , CM000668.2:g.44302065C= GRCh38
NC_000006.11:g.44269802C= , CM000668.1:g.44269802C= GRCh37
NC_000006.10:g.44377780C= NCBI36
NG_031952.1:g.16262G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2593G= (AARS2) MANE Select ENSP00000244571.4:p.Gly865=
ENST00000244571.4:c.2593G= (AARS2) ENSP00000244571.4:p.Gly865=
ENST00000438774.2:c.577-4878C= (TMEM151B) ENSP00000409337.2:n.577-4878C=
ENST00000505802.1:c.314-4878C=
NM_020745.3:c.2593G= (AARS2) NP_065796.1:p.Gly865=
XM_005249245.2:c.2302G= (AARS2) XP_005249302.1:p.Gly768=
XM_011514764.1:c.2593G= (AARS2) XP_011513066.1:p.Gly865=
XR_241907.2:n.2518G= (AARS2)
XM_005249245.3:c.2302G= (AARS2) XP_005249302.1:p.Gly768=
XM_011514764.2:c.2593G= (AARS2) XP_011513066.1:p.Gly865=
XM_017011112.1:c.1303G= (AARS2) XP_016866601.1:p.Gly435=
NM_020745.4:c.2593G= (AARS2) MANE Select NP_065796.2:p.Gly865=
NM_001318876.2:c.946-139825C= (POLR1C) NP_001305805.1:n.946-139825C=