Canonical Allele Identifier: CA1076975

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150498580C>T , CM000663.2:g.150498580C>T	GRCh38
NC_000001.10:g.150471056C>T , CM000663.1:g.150471056C>T	GRCh37
NC_000001.9:g.148737680C>T	NCBI36
NG_034226.1:g.16217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.1317C>T MANE Select	ENSP00000358060.3:p.Ala439=
ENST00000369051.7:c.*308C>T	ENSP00000358047.3:n.*308C>T
ENST00000369054.6:c.927C>T	ENSP00000358050.2:p.Ala309=
ENST00000369064.7:c.1317C>T	ENSP00000358060.3:p.Ala439=
ENST00000438568.6:c.492C>T	ENSP00000415002.3:p.Ala164=
ENST00000463555.1:n.450C>T
ENST00000467982.6:c.896C>T	ENSP00000475551.1:n.896C>T
ENST00000480070.5:n.430C>T
ENST00000606933.5:c.1071C>T	ENSP00000475847.1:p.Ala357=
NM_001271895.1:c.1071C>T	NP_001258824.1:p.Ala357=
NM_001271896.1:c.927C>T	NP_001258825.1:p.Ala309=
NM_025150.4:c.1317C>T	NP_079426.2:p.Ala439=
NR_073513.1:n.803C>T
NR_073514.1:n.1279C>T
XM_006711555.1:c.1317C>T	XP_006711618.1:p.Ala439=
XM_006711556.1:c.1170C>T	XP_006711619.1:p.Ala390=
XM_011510009.1:c.1218C>T	XP_011508311.1:p.Ala406=
XM_006711555.2:c.1317C>T	XP_006711618.1:p.Ala439=
XM_017002394.2:c.1170C>T	XP_016857883.1:p.Ala390=
XM_017002395.2:c.1071C>T	XP_016857884.1:p.Ala357=
NM_025150.5:c.1317C>T MANE Select	NP_079426.2:p.Ala439=
NM_001271895.2:c.1071C>T	NP_001258824.1:p.Ala357=
NM_001271896.2:c.927C>T	NP_001258825.1:p.Ala309=
NR_073513.2:n.748C>T
NR_073514.2:n.1224C>T