Canonical Allele Identifier: CA1077018

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150498948G>A , CM000663.2:g.150498948G>A	GRCh38
NC_000001.10:g.150471424G>A , CM000663.1:g.150471424G>A	GRCh37
NC_000001.9:g.148738048G>A	NCBI36
NG_034226.1:g.16585G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.1453G>A MANE Select	ENSP00000358060.3:p.Val485Ile
ENST00000369051.7:c.*444G>A	ENSP00000358047.3:n.*444G>A
ENST00000369054.6:c.1063G>A	ENSP00000358050.2:p.Val355Ile
ENST00000369064.7:c.1453G>A	ENSP00000358060.3:p.Val485Ile
ENST00000438568.6:c.628G>A	ENSP00000415002.3:p.Val210Ile
ENST00000463555.1:n.586G>A
ENST00000467982.6:c.1032G>A	ENSP00000475551.1:n.1032G>A
ENST00000480070.5:n.566G>A
ENST00000606933.5:c.1207G>A	ENSP00000475847.1:p.Val403Ile
NM_001271895.1:c.1207G>A	NP_001258824.1:p.Val403Ile
NM_001271896.1:c.1063G>A	NP_001258825.1:p.Val355Ile
NM_025150.4:c.1453G>A	NP_079426.2:p.Val485Ile
NR_073513.1:n.939G>A
NR_073514.1:n.1415G>A
XM_006711555.1:c.1453G>A	XP_006711618.1:p.Val485Ile
XM_006711556.1:c.1306G>A	XP_006711619.1:p.Val436Ile
XM_011510009.1:c.1354G>A	XP_011508311.1:p.Val452Ile
XM_006711555.2:c.1453G>A	XP_006711618.1:p.Val485Ile
XM_017002394.2:c.1306G>A	XP_016857883.1:p.Val436Ile
XM_017002395.2:c.1207G>A	XP_016857884.1:p.Val403Ile
NM_025150.5:c.1453G>A MANE Select	NP_079426.2:p.Val485Ile
NM_001271895.2:c.1207G>A	NP_001258824.1:p.Val403Ile
NM_001271896.2:c.1063G>A	NP_001258825.1:p.Val355Ile
NR_073513.2:n.884G>A
NR_073514.2:n.1360G>A