Canonical Allele Identifier: CA1624922856

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44302072C= , CM000668.2:g.44302072C= GRCh38
NC_000006.11:g.44269809C= , CM000668.1:g.44269809C= GRCh37
NC_000006.10:g.44377787C= NCBI36
NG_031952.1:g.16255G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2586G= (AARS2) MANE Select ENSP00000244571.4:p.Leu862=
ENST00000244571.4:c.2586G= (AARS2) ENSP00000244571.4:p.Leu862=
ENST00000438774.2:c.577-4871C= (TMEM151B) ENSP00000409337.2:n.577-4871C=
ENST00000505802.1:c.314-4871C=
NM_020745.3:c.2586G= (AARS2) NP_065796.1:p.Leu862=
XM_005249245.2:c.2295G= (AARS2) XP_005249302.1:p.Leu765=
XM_011514764.1:c.2586G= (AARS2) XP_011513066.1:p.Leu862=
XR_241907.2:n.2511G= (AARS2)
XM_005249245.3:c.2295G= (AARS2) XP_005249302.1:p.Leu765=
XM_011514764.2:c.2586G= (AARS2) XP_011513066.1:p.Leu862=
XM_017011112.1:c.1296G= (AARS2) XP_016866601.1:p.Leu432=
NM_020745.4:c.2586G= (AARS2) MANE Select NP_065796.2:p.Leu862=
NM_001318876.2:c.946-139818C= (POLR1C) NP_001305805.1:n.946-139818C=