Canonical Allele Identifier: CA1624921762

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44300512C= , CM000668.2:g.44300512C= GRCh38
NC_000006.11:g.44268249C= , CM000668.1:g.44268249C= GRCh37
NC_000006.10:g.44376227C= NCBI36
NG_031952.1:g.17815G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.*35G= (AARS2) MANE Select ENSP00000244571.4:n.*35G=
ENST00000244571.4:c.*35G= (AARS2) ENSP00000244571.4:n.*35G=
ENST00000438774.2:c.577-6431C= (TMEM151B) ENSP00000409337.2:n.577-6431C=
ENST00000505802.1:c.314-6431C=
NM_020745.3:c.*35G= (AARS2) NP_065796.1:n.*35G=
XM_005249245.2:c.*35G= (AARS2) XP_005249302.1:n.*35G=
XM_011514764.1:c.2793+644G= (AARS2) XP_011513066.1:n.2793+644G=
XR_241907.2:n.2918G= (AARS2)
XM_005249245.3:c.*35G= (AARS2) XP_005249302.1:n.*35G=
XM_011514764.2:c.2793+644G= (AARS2) XP_011513066.1:n.2793+644G=
XM_017011112.1:c.*35G= (AARS2) XP_016866601.1:n.*35G=
NM_020745.4:c.*35G= (AARS2) MANE Select NP_065796.2:n.*35G=
NM_001318876.2:c.946-141378C= (POLR1C) NP_001305805.1:n.946-141378C=