Canonical Allele Identifier: CA1624923942

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303068C= , CM000668.2:g.44303068C= GRCh38
NC_000006.11:g.44270805C= , CM000668.1:g.44270805C= GRCh37
NC_000006.10:g.44378783C= NCBI36
NG_031952.1:g.15259G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244571.5:c.2253G= (AARS2) MANE Select ENSP00000244571.4:p.Gly751=
ENST00000244571.4:c.2253G= (AARS2) ENSP00000244571.4:p.Gly751=
ENST00000438774.2:c.577-3875C= (TMEM151B) ENSP00000409337.2:n.577-3875C=
ENST00000505802.1:c.314-3875C=
NM_020745.3:c.2253G= (AARS2) NP_065796.1:p.Gly751=
XM_005249245.2:c.1962G= (AARS2) XP_005249302.1:p.Gly654=
XM_011514764.1:c.2253G= (AARS2) XP_011513066.1:p.Gly751=
XR_241907.2:n.2181-158G= (AARS2)
XM_005249245.3:c.1962G= (AARS2) XP_005249302.1:p.Gly654=
XM_011514764.2:c.2253G= (AARS2) XP_011513066.1:p.Gly751=
XM_017011112.1:c.963G= (AARS2) XP_016866601.1:p.Gly321=
NM_020745.4:c.2253G= (AARS2) MANE Select NP_065796.2:p.Gly751=
NM_001318876.2:c.946-138822C= (POLR1C) NP_001305805.1:n.946-138822C=