Canonical Allele Identifier: CA16603427

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150507049C>T , CM000663.2:g.150507049C>T	GRCh38
NC_000001.10:g.150479525C>T , CM000663.1:g.150479525C>T	GRCh37
NC_000001.9:g.148746149C>T	NCBI36
NG_012062.1:g.4039C>T
NG_034226.1:g.24686C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.2142C>T MANE Select	ENSP00000358060.3:p.Ala714=
ENST00000369051.7:c.*1133C>T	ENSP00000358047.3:n.*1133C>T
ENST00000369054.6:c.1752C>T	ENSP00000358050.2:p.Ala584=
ENST00000369064.7:c.2142C>T	ENSP00000358060.3:p.Ala714=
ENST00000438568.6:c.1317C>T	ENSP00000415002.3:p.Ala439=
ENST00000467982.6:c.1721C>T	ENSP00000475551.1:n.1721C>T
ENST00000606933.5:c.1896C>T	ENSP00000475847.1:p.Ala632=
NM_001271895.1:c.1896C>T	NP_001258824.1:p.Ala632=
NM_001271896.1:c.1752C>T	NP_001258825.1:p.Ala584=
NM_025150.4:c.2142C>T	NP_079426.2:p.Ala714=
NR_073513.1:n.1628C>T
NR_073514.1:n.2104C>T
XM_006711555.1:c.2040C>T	XP_006711618.1:p.Ala680=
XM_006711556.1:c.1995C>T	XP_006711619.1:p.Ala665=
XM_011510009.1:c.2043C>T	XP_011508311.1:p.Ala681=
XM_006711555.2:c.2040C>T	XP_006711618.1:p.Ala680=
XM_017002394.2:c.1893C>T	XP_016857883.1:p.Ala631=
XM_017002395.2:c.1794C>T	XP_016857884.1:p.Ala598=
NM_025150.5:c.2142C>T MANE Select	NP_079426.2:p.Ala714=
NM_001271895.2:c.1896C>T	NP_001258824.1:p.Ala632=
NM_001271896.2:c.1752C>T	NP_001258825.1:p.Ala584=
NR_073513.2:n.1573C>T
NR_073514.2:n.2049C>T