Canonical Allele Identifier: CA1076831

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150496607G>C , CM000663.2:g.150496607G>C	GRCh38
NC_000001.10:g.150469083G>C , CM000663.1:g.150469083G>C	GRCh37
NC_000001.9:g.148735707G>C	NCBI36
NG_034226.1:g.14244G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.900G>C MANE Select	ENSP00000358060.3:p.Arg300=
ENST00000369051.7:c.*12-923G>C	ENSP00000358047.3:n.*12-923G>C
ENST00000369054.6:c.631-923G>C	ENSP00000358050.2:n.631-923G>C
ENST00000369064.7:c.900G>C	ENSP00000358060.3:p.Arg300=
ENST00000438568.6:c.196-923G>C	ENSP00000415002.3:n.196-923G>C
ENST00000460794.1:n.501-923G>C
ENST00000462578.1:n.431G>C
ENST00000463555.1:n.154-923G>C
ENST00000467982.6:c.697G>C	ENSP00000475551.1:n.697G>C
ENST00000480070.5:n.134-923G>C
ENST00000606933.5:c.775-923G>C	ENSP00000475847.1:n.775-923G>C
NM_001271895.1:c.775-923G>C	NP_001258824.1:n.775-923G>C
NM_001271896.1:c.631-923G>C	NP_001258825.1:n.631-923G>C
NM_025150.4:c.900G>C	NP_079426.2:p.Arg300=
NR_073513.1:n.507-923G>C
NR_073514.1:n.862G>C
XM_006711555.1:c.900G>C	XP_006711618.1:p.Arg300=
XM_006711556.1:c.775-203G>C	XP_006711619.1:n.775-203G>C
XM_011510009.1:c.900G>C	XP_011508311.1:p.Arg300=
XM_006711555.2:c.900G>C	XP_006711618.1:p.Arg300=
XM_017002394.2:c.775-203G>C	XP_016857883.1:n.775-203G>C
XM_017002395.2:c.775-923G>C	XP_016857884.1:n.775-923G>C
NM_025150.5:c.900G>C MANE Select	NP_079426.2:p.Arg300=
NM_001271895.2:c.775-923G>C	NP_001258824.1:n.775-923G>C
NM_001271896.2:c.631-923G>C	NP_001258825.1:n.631-923G>C
NR_073513.2:n.452-923G>C
NR_073514.2:n.807G>C