Canonical Allele Identifier: CA30061501

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150491804del , CM000663.2:g.150491804del	GRCh38
NC_000001.10:g.150464280del , CM000663.1:g.150464280del	GRCh37
NC_000001.9:g.148730904del	NCBI36
NG_034226.1:g.9441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.695+142del MANE Select	ENSP00000358060.3:n.695+142del
ENST00000369051.7:c.341-607del	ENSP00000358047.3:n.341-607del
ENST00000369054.6:c.630+293del	ENSP00000358050.2:n.630+293del
ENST00000369064.7:c.695+142del	ENSP00000358060.3:n.695+142del
ENST00000438568.6:c.117-607del	ENSP00000415002.3:n.117-607del
ENST00000463555.1:n.74+142del
ENST00000467982.6:c.492+142del	ENSP00000475551.1:n.492+142del
ENST00000480070.5:n.54+293del
ENST00000606933.5:c.695+142del	ENSP00000475847.1:n.695+142del
NM_001271895.1:c.695+142del	NP_001258824.1:n.695+142del
NM_001271896.1:c.630+293del	NP_001258825.1:n.630+293del
NM_025150.4:c.695+142del	NP_079426.2:n.695+142del
NR_073513.1:n.428-607del
NR_073514.1:n.657+142del
XM_006711555.1:c.695+142del	XP_006711618.1:n.695+142del
XM_006711556.1:c.695+142del	XP_006711619.1:n.695+142del
XM_011510009.1:c.695+142del	XP_011508311.1:n.695+142del
XM_006711555.2:c.695+142del	XP_006711618.1:n.695+142del
XM_017002394.2:c.695+142del	XP_016857883.1:n.695+142del
XM_017002395.2:c.695+142del	XP_016857884.1:n.695+142del
NM_025150.5:c.695+142del MANE Select	NP_079426.2:n.695+142del
NM_001271895.2:c.695+142del	NP_001258824.1:n.695+142del
NM_001271896.2:c.630+293del	NP_001258825.1:n.630+293del
NR_073513.2:n.373-607del
NR_073514.2:n.602+142del