Canonical Allele Identifier: CA1624921809

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44300613G= , CM000668.2:g.44300613G= GRCh38
NC_000006.11:g.44268350G= , CM000668.1:g.44268350G= GRCh37
NC_000006.10:g.44376328G= NCBI36
NG_031952.1:g.17714C=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2892C= (AARS2) MANE Select ENSP00000244571.4:p.Thr964=
ENST00000244571.4:c.2892C= (AARS2) ENSP00000244571.4:p.Thr964=
ENST00000438774.2:c.577-6330G= (TMEM151B) ENSP00000409337.2:n.577-6330G=
ENST00000491573.1:n.694C= (AARS2)
ENST00000505802.1:c.314-6330G=
NM_020745.3:c.2892C= (AARS2) NP_065796.1:p.Thr964=
XM_005249245.2:c.2601C= (AARS2) XP_005249302.1:p.Thr867=
XM_011514764.1:c.2793+543C= (AARS2) XP_011513066.1:n.2793+543C=
XR_241907.2:n.2817C= (AARS2)
XM_005249245.3:c.2601C= (AARS2) XP_005249302.1:p.Thr867=
XM_011514764.2:c.2793+543C= (AARS2) XP_011513066.1:n.2793+543C=
XM_017011112.1:c.1602C= (AARS2) XP_016866601.1:p.Thr534=
NM_020745.4:c.2892C= (AARS2) MANE Select NP_065796.2:p.Thr964=
NM_001318876.2:c.946-141277G= (POLR1C) NP_001305805.1:n.946-141277G=