Canonical Allele Identifier: CA1586866892

Gene: HARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695800G= , CM000667.2:g.140695800G=	GRCh38
NC_000005.9:g.140075385G= , CM000667.1:g.140075385G=	GRCh37
NC_000005.8:g.140055569G=	NCBI36
NG_021415.1:g.9368G=
NG_032158.1:g.587C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.588G= MANE Select	ENSP00000230771.3:p.Met196=
ENST00000503873.6:c.366G=	ENSP00000424516.2:p.Met122=
ENST00000509299.6:c.378G=	ENSP00000425695.2:p.Met126=
ENST00000520095.6:c.*166G=	ENSP00000429220.1:n.*166G=
ENST00000642452.1:c.554G=
ENST00000642752.1:c.588G=	ENSP00000493630.1:p.Met196=
ENST00000642970.1:c.378G=	ENSP00000496011.1:p.Met126=
ENST00000643996.1:c.378G=	ENSP00000495350.1:p.Met126=
ENST00000645065.1:c.606G=	ENSP00000493571.1:p.Met202=
ENST00000645749.1:c.588G=	ENSP00000494296.1:p.Met196=
ENST00000646468.1:c.606G=	ENSP00000494965.1:p.Met202=
ENST00000647484.1:c.378G=	ENSP00000494140.1:p.Met126=
ENST00000230771.7:c.588G=	ENSP00000230771.3:p.Met196=
ENST00000448069.2:c.171G=	ENSP00000407105.2:p.Met57=
ENST00000508522.5:c.513G=	ENSP00000423616.1:p.Met171=
ENST00000510104.5:c.*388G=	ENSP00000423530.1:n.*388G=
ENST00000513688.1:n.595G=
NM_001278731.1:c.513G=	NP_001265660.1:p.Met171=
NM_001278732.1:c.156G=	NP_001265661.1:p.Met52=
NM_012208.3:c.588G=	NP_036340.1:p.Met196=
XM_011537619.1:c.606G=	XP_011535921.1:p.Met202=
XM_011537620.1:c.606G=	XP_011535922.1:p.Met202=
NM_001363535.1:c.606G=	NP_001350464.1:p.Met202=
NM_001363536.1:c.378G=	NP_001350465.1:p.Met126=
XM_017009288.1:c.378G=	XP_016864777.1:p.Met126=
XM_017009289.1:c.378G=	XP_016864778.1:p.Met126=
XM_017009290.2:c.-147G=	XP_016864779.1:n.-147G=
XM_017009291.1:c.-147G=	XP_016864780.1:n.-147G=
XM_017009292.1:c.-147G=	XP_016864781.1:n.-147G=
NM_012208.4:c.588G= MANE Select	NP_036340.1:p.Met196=
NM_001278731.2:c.513G=	NP_001265660.1:p.Met171=
NM_001278732.2:c.156G=	NP_001265661.1:p.Met52=
NM_001363535.2:c.606G=	NP_001350464.1:p.Met202=
NM_001363536.2:c.378G=	NP_001350465.1:p.Met126=