Canonical Allele Identifier: CA359371749

Gene: TARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33456216A>G , CM000667.2:g.33456216A>G	GRCh38
NC_000005.9:g.33456321A>G , CM000667.1:g.33456321A>G	GRCh37
NC_000005.8:g.33492078A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152295.5:c.826A>G MANE Select	NP_689508.3:p.Lys276Glu
ENST00000265112.8:c.826A>G MANE Select	ENSP00000265112.3:p.Lys276Glu
NM_001258437.1:c.826A>G	NP_001245366.1:p.Lys276Glu
NM_001258438.1:c.925A>G	NP_001245367.1:p.Lys309Glu
NM_001258438.2:c.925A>G	NP_001245367.1:p.Lys309Glu
NM_152295.4:c.826A>G	NP_689508.3:p.Lys276Glu
NR_047676.1:n.1258A>G
NR_047676.2:n.1069A>G
NR_047677.1:n.976A>G
NR_047677.2:n.787A>G
NR_047678.1:n.946A>G
NR_047678.2:n.757A>G
ENST00000265112.7:c.826A>G	ENSP00000265112.3:p.Lys276Glu
ENST00000455217.6:c.925A>G	ENSP00000387710.2:p.Lys309Glu
ENST00000502553.5:c.826A>G	ENSP00000424387.1:p.Lys276Glu
ENST00000504698.1:n.101A>G
ENST00000507716.5:c.*269A>G	ENSP00000420893.1:n.*269A>G
ENST00000508361.5:c.*464A>G	ENSP00000427627.1:n.*464A>G
ENST00000509731.5:c.*779A>G	ENSP00000427304.1:n.*779A>G