Canonical Allele Identifier: CA364336416

Gene: AARS2 TMEM151B POLR1C

Linked Data

• COSMIC: COSM3874427
• MyVariant Identifiers: chr6:g.44269806T>G (hg19) ; chr6:g.44302069T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44302069T>G , CM000668.2:g.44302069T>G	GRCh38
NC_000006.11:g.44269806T>G , CM000668.1:g.44269806T>G	GRCh37
NC_000006.10:g.44377784T>G	NCBI36
NG_031952.1:g.16258A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000244571.5:c.2589A>C (AARS2) MANE Select	ENSP00000244571.4:p.Gln863His
ENST00000244571.4:c.2589A>C (AARS2)	ENSP00000244571.4:p.Gln863His
ENST00000438774.2:c.577-4874T>G (TMEM151B)	ENSP00000409337.2:n.577-4874T>G
ENST00000505802.1:c.314-4874T>G
NM_020745.3:c.2589A>C (AARS2)	NP_065796.1:p.Gln863His
XM_005249245.2:c.2298A>C (AARS2)	XP_005249302.1:p.Gln766His
XM_011514764.1:c.2589A>C (AARS2)	XP_011513066.1:p.Gln863His
XR_241907.2:n.2514A>C (AARS2)
XM_005249245.3:c.2298A>C (AARS2)	XP_005249302.1:p.Gln766His
XM_011514764.2:c.2589A>C (AARS2)	XP_011513066.1:p.Gln863His
XM_017011112.1:c.1299A>C (AARS2)	XP_016866601.1:p.Gln433His
NM_020745.4:c.2589A>C (AARS2) MANE Select	NP_065796.2:p.Gln863His
NM_001318876.2:c.946-139821T>G (POLR1C)	NP_001305805.1:n.946-139821T>G