Canonical Allele Identifier: CA1624923934

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303066G= , CM000668.2:g.44303066G= GRCh38
NC_000006.11:g.44270803G= , CM000668.1:g.44270803G= GRCh37
NC_000006.10:g.44378781G= NCBI36
NG_031952.1:g.15261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2255C= (AARS2) MANE Select ENSP00000244571.4:p.Thr752=
ENST00000244571.4:c.2255C= (AARS2) ENSP00000244571.4:p.Thr752=
ENST00000438774.2:c.577-3877G= (TMEM151B) ENSP00000409337.2:n.577-3877G=
ENST00000505802.1:c.314-3877G=
NM_020745.3:c.2255C= (AARS2) NP_065796.1:p.Thr752=
XM_005249245.2:c.1964C= (AARS2) XP_005249302.1:p.Thr655=
XM_011514764.1:c.2255C= (AARS2) XP_011513066.1:p.Thr752=
XR_241907.2:n.2181-156C= (AARS2)
XM_005249245.3:c.1964C= (AARS2) XP_005249302.1:p.Thr655=
XM_011514764.2:c.2255C= (AARS2) XP_011513066.1:p.Thr752=
XM_017011112.1:c.965C= (AARS2) XP_016866601.1:p.Thr322=
NM_020745.4:c.2255C= (AARS2) MANE Select NP_065796.2:p.Thr752=
NM_001318876.2:c.946-138824G= (POLR1C) NP_001305805.1:n.946-138824G=