Canonical Allele Identifier: CA30067186

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150499383dup , CM000663.2:g.150499383dup	GRCh38
NC_000001.10:g.150471859dup , CM000663.1:g.150471859dup	GRCh37
NC_000001.9:g.148738483dup	NCBI36
NG_034226.1:g.17020dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.1617+90dup MANE Select	ENSP00000358060.3:n.1617+90dup
ENST00000369051.7:c.*608+90dup	ENSP00000358047.3:n.*608+90dup
ENST00000369054.6:c.1227+90dup	ENSP00000358050.2:n.1227+90dup
ENST00000369064.7:c.1617+90dup	ENSP00000358060.3:n.1617+90dup
ENST00000438568.6:c.792+90dup	ENSP00000415002.3:n.792+90dup
ENST00000463555.1:n.750+90dup
ENST00000467982.6:c.1196+90dup	ENSP00000475551.1:n.1196+90dup
ENST00000480070.5:n.730+90dup
ENST00000606933.5:c.1371+90dup	ENSP00000475847.1:n.1371+90dup
NM_001271895.1:c.1371+90dup	NP_001258824.1:n.1371+90dup
NM_001271896.1:c.1227+90dup	NP_001258825.1:n.1227+90dup
NM_025150.4:c.1617+90dup	NP_079426.2:n.1617+90dup
NR_073513.1:n.1103+90dup
NR_073514.1:n.1579+90dup
XM_006711555.1:c.1617+90dup	XP_006711618.1:n.1617+90dup
XM_006711556.1:c.1470+90dup	XP_006711619.1:n.1470+90dup
XM_011510009.1:c.1518+90dup	XP_011508311.1:n.1518+90dup
XM_006711555.2:c.1617+90dup	XP_006711618.1:n.1617+90dup
XM_017002394.2:c.1470+90dup	XP_016857883.1:n.1470+90dup
XM_017002395.2:c.1371+90dup	XP_016857884.1:n.1371+90dup
NM_025150.5:c.1617+90dup MANE Select	NP_079426.2:n.1617+90dup
NM_001271895.2:c.1371+90dup	NP_001258824.1:n.1371+90dup
NM_001271896.2:c.1227+90dup	NP_001258825.1:n.1227+90dup
NR_073513.2:n.1048+90dup
NR_073514.2:n.1524+90dup