Canonical Allele Identifier: CA1586861407

Gene: HARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140674776T= , CM000667.2:g.140674776T=	GRCh38
NC_000005.9:g.140054361T= , CM000667.1:g.140054361T=	GRCh37
NC_000005.8:g.140034545T=	NCBI36
NG_032158.1:g.21611A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431330.7:c.1019A=	ENSP00000393244.2:p.Tyr340=
ENST00000504156.7:c.1361A= MANE Select	ENSP00000425634.1:p.Tyr454=
ENST00000506579.6:n.4106A=
ENST00000507746.7:c.1361A=	ENSP00000425889.2:p.Tyr454=
ENST00000509087.2:c.347A=	ENSP00000502781.1:p.Tyr116=
ENST00000512396.6:c.*1300A=	ENSP00000421576.1:n.*1300A=
ENST00000643686.1:c.*1416A=	ENSP00000493611.1:n.*1416A=
ENST00000645491.1:c.*1294A=	ENSP00000494297.1:n.*1294A=
ENST00000646229.1:c.1412A=
ENST00000674523.1:c.*651A=	ENSP00000501816.1:n.*651A=
ENST00000675094.1:n.2458A=
ENST00000675204.1:c.1361A=	ENSP00000501643.1:p.Tyr454=
ENST00000675355.1:n.1146A=
ENST00000675366.1:c.1244A=	ENSP00000501747.1:p.Tyr415=
ENST00000675698.1:c.1154A=	ENSP00000501581.1:p.Tyr385=
ENST00000675763.1:n.3268A=
ENST00000675827.1:c.*454A=	ENSP00000501900.1:n.*454A=
ENST00000675851.1:c.1031A=	ENSP00000502624.1:p.Tyr344=
ENST00000675898.1:n.3179A=
ENST00000675967.1:n.2975A=
ENST00000676327.1:c.1253A=	ENSP00000502594.1:p.Tyr418=
ENST00000307633.7:c.1181A=	ENSP00000304668.3:p.Tyr394=
ENST00000415192.6:c.1139A=	ENSP00000411085.2:p.Tyr380=
ENST00000431330.6:c.1019A=	ENSP00000393244.2:p.Tyr340=
ENST00000438307.6:c.1241A=	ENSP00000411511.2:p.Tyr414=
ENST00000457527.6:c.1301A=	ENSP00000387893.2:p.Tyr434=
ENST00000504156.5:c.1361A=	ENSP00000425634.1:p.Tyr454=
ENST00000504366.5:c.1154A=	ENSP00000430063.1:p.Tyr385=
ENST00000509087.1:n.367A=
NM_001258040.2:c.1241A=	NP_001244969.1:p.Tyr414=
NM_001258041.2:c.1301A=	NP_001244970.1:p.Tyr434=
NM_001258042.2:c.1181A=	NP_001244971.1:p.Tyr394=
NM_001289092.1:c.1139A=	NP_001276021.1:p.Tyr380=
NM_001289093.1:c.1019A=	NP_001276022.1:p.Tyr340=
NM_001289094.1:c.1274A=	NP_001276023.1:p.Tyr425=
NM_002109.5:c.1361A=	NP_002100.2:p.Tyr454=
NM_002109.6:c.1361A= MANE Select	NP_002100.2:p.Tyr454=
NM_001258040.3:c.1241A=	NP_001244969.1:p.Tyr414=
NM_001258041.3:c.1301A=	NP_001244970.1:p.Tyr434=
NM_001258042.3:c.1181A=	NP_001244971.1:p.Tyr394=
NM_001289092.2:c.1139A=	NP_001276021.1:p.Tyr380=
NM_001289093.2:c.1019A=	NP_001276022.1:p.Tyr340=
NM_001289094.2:c.1274A=	NP_001276023.1:p.Tyr425=