Canonical Allele Identifier: CA1624924078

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44303139C= , CM000668.2:g.44303139C= GRCh38
NC_000006.11:g.44270876C= , CM000668.1:g.44270876C= GRCh37
NC_000006.10:g.44378854C= NCBI36
NG_031952.1:g.15188G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.2182G= (AARS2) MANE Select ENSP00000244571.4:p.Val728=
ENST00000244571.4:c.2182G= (AARS2) ENSP00000244571.4:p.Val728=
ENST00000438774.2:c.577-3804C= (TMEM151B) ENSP00000409337.2:n.577-3804C=
ENST00000505802.1:c.314-3804C=
NM_020745.3:c.2182G= (AARS2) NP_065796.1:p.Val728=
XM_005249245.2:c.1891G= (AARS2) XP_005249302.1:p.Val631=
XM_011514764.1:c.2182G= (AARS2) XP_011513066.1:p.Val728=
XR_241907.2:n.2180+147G= (AARS2)
XM_005249245.3:c.1891G= (AARS2) XP_005249302.1:p.Val631=
XM_011514764.2:c.2182G= (AARS2) XP_011513066.1:p.Val728=
XM_017011112.1:c.892G= (AARS2) XP_016866601.1:p.Val298=
NM_020745.4:c.2182G= (AARS2) MANE Select NP_065796.2:p.Val728=
NM_001318876.2:c.946-138751C= (POLR1C) NP_001305805.1:n.946-138751C=