Canonical Allele Identifier: CA1624924416

Gene: AARS2 TMEM151B POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44303373_44303374delinsCT , CM000668.2:g.44303373_44303374delinsCT	GRCh38
NC_000006.11:g.44271110_44271111delinsCT , CM000668.1:g.44271110_44271111delinsCT	GRCh37
NC_000006.10:g.44379088_44379089delinsCT	NCBI36
NG_031952.1:g.14953_14954delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244571.5:c.2057_2058delinsAG (AARS2) MANE Select	ENSP00000244571.4:p.Glu686=
ENST00000244571.4:c.2057_2058delinsAG (AARS2)	ENSP00000244571.4:p.Glu686=
ENST00000438774.2:c.577-3570_577-3569delinsCT (TMEM151B)	ENSP00000409337.2:n.577-3570_577-3569delinsCT
ENST00000505802.1:c.314-3570_314-3569delinsCT
NM_020745.3:c.2057_2058delinsAG (AARS2)	NP_065796.1:p.Glu686=
XM_005249245.2:c.1766_1767delinsAG (AARS2)	XP_005249302.1:p.Glu589=
XM_011514764.1:c.2057_2058delinsAG (AARS2)	XP_011513066.1:p.Glu686=
XR_241907.2:n.2092_2093delinsAG (AARS2)
XM_005249245.3:c.1766_1767delinsAG (AARS2)	XP_005249302.1:p.Glu589=
XM_011514764.2:c.2057_2058delinsAG (AARS2)	XP_011513066.1:p.Glu686=
XM_017011112.1:c.767_768delinsAG (AARS2)	XP_016866601.1:p.Glu256=
NM_020745.4:c.2057_2058delinsAG (AARS2) MANE Select	NP_065796.2:p.Glu686=
NM_001318876.2:c.946-138517_946-138516delinsCT (POLR1C)	NP_001305805.1:n.946-138517_946-138516delinsCT