Canonical Allele Identifier: CA1076869

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150496856T>G , CM000663.2:g.150496856T>G	GRCh38
NC_000001.10:g.150469332T>G , CM000663.1:g.150469332T>G	GRCh37
NC_000001.9:g.148735956T>G	NCBI36
NG_034226.1:g.14493T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025150.5:c.968T>G MANE Select	NP_079426.2:p.Phe323Cys
ENST00000369064.8:c.968T>G MANE Select	ENSP00000358060.3:p.Phe323Cys
NM_001271895.1:c.775-674T>G	NP_001258824.1:n.775-674T>G
NM_001271895.2:c.775-674T>G	NP_001258824.1:n.775-674T>G
NM_001271896.1:c.631-674T>G	NP_001258825.1:n.631-674T>G
NM_001271896.2:c.631-674T>G	NP_001258825.1:n.631-674T>G
NM_025150.4:c.968T>G	NP_079426.2:p.Phe323Cys
NR_073513.1:n.507-674T>G
NR_073513.2:n.452-674T>G
NR_073514.1:n.930T>G
NR_073514.2:n.875T>G
ENST00000369051.7:c.*12-674T>G	ENSP00000358047.3:n.*12-674T>G
ENST00000369054.6:c.631-674T>G	ENSP00000358050.2:n.631-674T>G
ENST00000369064.7:c.968T>G	ENSP00000358060.3:p.Phe323Cys
ENST00000438568.6:c.196-674T>G	ENSP00000415002.3:n.196-674T>G
ENST00000460794.1:n.501-674T>G
ENST00000462578.1:n.499T>G
ENST00000463555.1:n.154-674T>G
ENST00000467982.6:c.765T>G	ENSP00000475551.1:n.765T>G
ENST00000480070.5:n.134-674T>G
ENST00000606933.5:c.775-674T>G	ENSP00000475847.1:n.775-674T>G
XM_006711555.1:c.968T>G	XP_006711618.1:p.Phe323Cys
XM_006711555.2:c.968T>G	XP_006711618.1:p.Phe323Cys
XM_006711556.1:c.821T>G	XP_006711619.1:p.Phe274Cys
XM_011510009.1:c.921+228T>G	XP_011508311.1:n.921+228T>G
XM_017002394.2:c.821T>G	XP_016857883.1:p.Phe274Cys
XM_017002395.2:c.775-674T>G	XP_016857884.1:n.775-674T>G