Canonical Allele Identifier: CA1586867015

Gene: HARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695843A= , CM000667.2:g.140695843A=	GRCh38
NC_000005.9:g.140075428A= , CM000667.1:g.140075428A=	GRCh37
NC_000005.8:g.140055612A=	NCBI36
NG_021415.1:g.9411A=
NG_032158.1:g.544T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.631A= MANE Select	ENSP00000230771.3:p.Lys211=
ENST00000503873.6:c.409A=	ENSP00000424516.2:p.Lys137=
ENST00000509299.6:c.421A=	ENSP00000425695.2:p.Lys141=
ENST00000520095.6:c.*209A=	ENSP00000429220.1:n.*209A=
ENST00000642452.1:c.597A=
ENST00000642752.1:c.631A=	ENSP00000493630.1:p.Lys211=
ENST00000642970.1:c.421A=	ENSP00000496011.1:p.Lys141=
ENST00000643996.1:c.421A=	ENSP00000495350.1:p.Lys141=
ENST00000645065.1:c.649A=	ENSP00000493571.1:p.Lys217=
ENST00000645749.1:c.631A=	ENSP00000494296.1:p.Lys211=
ENST00000646468.1:c.649A=	ENSP00000494965.1:p.Lys217=
ENST00000647484.1:c.421A=	ENSP00000494140.1:p.Lys141=
ENST00000230771.7:c.631A=	ENSP00000230771.3:p.Lys211=
ENST00000448069.2:c.214A=	ENSP00000407105.2:p.Lys72=
ENST00000508522.5:c.556A=	ENSP00000423616.1:p.Lys186=
ENST00000510104.5:c.*431A=	ENSP00000423530.1:n.*431A=
ENST00000513688.1:n.638A=
NM_001278731.1:c.556A=	NP_001265660.1:p.Lys186=
NM_001278732.1:c.199A=	NP_001265661.1:p.Lys67=
NM_012208.3:c.631A=	NP_036340.1:p.Lys211=
XM_011537619.1:c.649A=	XP_011535921.1:p.Lys217=
XM_011537620.1:c.649A=	XP_011535922.1:p.Lys217=
NM_001363535.1:c.649A=	NP_001350464.1:p.Lys217=
NM_001363536.1:c.421A=	NP_001350465.1:p.Lys141=
XM_017009288.1:c.421A=	XP_016864777.1:p.Lys141=
XM_017009289.1:c.421A=	XP_016864778.1:p.Lys141=
XM_017009290.2:c.-104A=	XP_016864779.1:n.-104A=
XM_017009291.1:c.-104A=	XP_016864780.1:n.-104A=
XM_017009292.1:c.-104A=	XP_016864781.1:n.-104A=
NM_012208.4:c.631A= MANE Select	NP_036340.1:p.Lys211=
NM_001278731.2:c.556A=	NP_001265660.1:p.Lys186=
NM_001278732.2:c.199A=	NP_001265661.1:p.Lys67=
NM_001363535.2:c.649A=	NP_001350464.1:p.Lys217=
NM_001363536.2:c.421A=	NP_001350465.1:p.Lys141=