Canonical Allele Identifier: CA1624923620

Gene: AARS2 TMEM151B POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302821G= , CM000668.2:g.44302821G=	GRCh38
NC_000006.11:g.44270558G= , CM000668.1:g.44270558G=	GRCh37
NC_000006.10:g.44378536G=	NCBI36
NG_031952.1:g.15506C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020745.4:c.2345C= (AARS2) MANE Select	NP_065796.2:p.Thr782=
ENST00000244571.5:c.2345C= (AARS2) MANE Select	ENSP00000244571.4:p.Thr782=
NM_001318876.2:c.946-139069G= (POLR1C)	NP_001305805.1:n.946-139069G=
NM_020745.3:c.2345C= (AARS2)	NP_065796.1:p.Thr782=
ENST00000244571.4:c.2345C= (AARS2)	ENSP00000244571.4:p.Thr782=
ENST00000438774.2:c.577-4122G= (TMEM151B)	ENSP00000409337.2:n.577-4122G=
ENST00000505802.1:c.314-4122G=
XM_005249245.2:c.2054C= (AARS2)	XP_005249302.1:p.Thr685=
XM_005249245.3:c.2054C= (AARS2)	XP_005249302.1:p.Thr685=
XM_011514764.1:c.2345C= (AARS2)	XP_011513066.1:p.Thr782=
XM_011514764.2:c.2345C= (AARS2)	XP_011513066.1:p.Thr782=
XM_017011112.1:c.1055C= (AARS2)	XP_016866601.1:p.Thr352=
XR_241907.2:n.2270C= (AARS2)