Canonical Allele Identifier: CA1077155

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150504725G>C , CM000663.2:g.150504725G>C	GRCh38
NC_000001.10:g.150477201G>C , CM000663.1:g.150477201G>C	GRCh37
NC_000001.9:g.148743825G>C	NCBI36
NG_012062.1:g.1715G>C
NG_034226.1:g.22362G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.1812G>C MANE Select	ENSP00000358060.3:p.Gly604=
ENST00000369051.7:c.*803G>C	ENSP00000358047.3:n.*803G>C
ENST00000369054.6:c.1422G>C	ENSP00000358050.2:p.Gly474=
ENST00000369064.7:c.1812G>C	ENSP00000358060.3:p.Gly604=
ENST00000438568.6:c.987G>C	ENSP00000415002.3:p.Gly329=
ENST00000467982.6:c.1391G>C	ENSP00000475551.1:n.1391G>C
ENST00000483046.1:n.104-181G>C
ENST00000606933.5:c.1566G>C	ENSP00000475847.1:p.Gly522=
NM_001271895.1:c.1566G>C	NP_001258824.1:p.Gly522=
NM_001271896.1:c.1422G>C	NP_001258825.1:p.Gly474=
NM_025150.4:c.1812G>C	NP_079426.2:p.Gly604=
NR_073513.1:n.1298G>C
NR_073514.1:n.1774G>C
XM_006711555.1:c.1719-181G>C	XP_006711618.1:n.1719-181G>C
XM_006711556.1:c.1665G>C	XP_006711619.1:p.Gly555=
XM_011510009.1:c.1713G>C	XP_011508311.1:p.Gly571=
XM_006711555.2:c.1719-181G>C	XP_006711618.1:n.1719-181G>C
XM_017002394.2:c.1572-181G>C	XP_016857883.1:n.1572-181G>C
XM_017002395.2:c.1473-181G>C	XP_016857884.1:n.1473-181G>C
NM_025150.5:c.1812G>C MANE Select	NP_079426.2:p.Gly604=
NM_001271895.2:c.1566G>C	NP_001258824.1:p.Gly522=
NM_001271896.2:c.1422G>C	NP_001258825.1:p.Gly474=
NR_073513.2:n.1243G>C
NR_073514.2:n.1719G>C