Canonical Allele Identifier: CA2841438405

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44300532del , CM000668.2:g.44300532del GRCh38
NC_000006.11:g.44268269del , CM000668.1:g.44268269del GRCh37
NC_000006.10:g.44376247del NCBI36
NG_031952.1:g.17797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.*17del (AARS2) MANE Select ENSP00000244571.4:n.*17del
ENST00000244571.4:c.*17del (AARS2) ENSP00000244571.4:n.*17del
ENST00000438774.2:c.577-6411del (TMEM151B) ENSP00000409337.2:n.577-6411del
ENST00000505802.1:c.314-6411del
NM_020745.3:c.*17del (AARS2) NP_065796.1:n.*17del
XM_005249245.2:c.*17del (AARS2) XP_005249302.1:n.*17del
XM_011514764.1:c.2793+626del (AARS2) XP_011513066.1:n.2793+626del
XR_241907.2:n.2900del (AARS2)
XM_005249245.3:c.*17del (AARS2) XP_005249302.1:n.*17del
XM_011514764.2:c.2793+626del (AARS2) XP_011513066.1:n.2793+626del
XM_017011112.1:c.*17del (AARS2) XP_016866601.1:n.*17del
NM_020745.4:c.*17del (AARS2) MANE Select NP_065796.2:n.*17del
NM_001318876.2:c.946-141358del (POLR1C) NP_001305805.1:n.946-141358del