Canonical Allele Identifier: CA1586866935

Gene: HARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695813A= , CM000667.2:g.140695813A=	GRCh38
NC_000005.9:g.140075398A= , CM000667.1:g.140075398A=	GRCh37
NC_000005.8:g.140055582A=	NCBI36
NG_021415.1:g.9381A=
NG_032158.1:g.574T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.601A= MANE Select	ENSP00000230771.3:p.Ser201=
ENST00000503873.6:c.379A=	ENSP00000424516.2:p.Ser127=
ENST00000509299.6:c.391A=	ENSP00000425695.2:p.Ser131=
ENST00000520095.6:c.*179A=	ENSP00000429220.1:n.*179A=
ENST00000642452.1:c.567A=
ENST00000642752.1:c.601A=	ENSP00000493630.1:p.Ser201=
ENST00000642970.1:c.391A=	ENSP00000496011.1:p.Ser131=
ENST00000643996.1:c.391A=	ENSP00000495350.1:p.Ser131=
ENST00000645065.1:c.619A=	ENSP00000493571.1:p.Ser207=
ENST00000645749.1:c.601A=	ENSP00000494296.1:p.Ser201=
ENST00000646468.1:c.619A=	ENSP00000494965.1:p.Ser207=
ENST00000647484.1:c.391A=	ENSP00000494140.1:p.Ser131=
ENST00000230771.7:c.601A=	ENSP00000230771.3:p.Ser201=
ENST00000448069.2:c.184A=	ENSP00000407105.2:p.Ser62=
ENST00000508522.5:c.526A=	ENSP00000423616.1:p.Ser176=
ENST00000510104.5:c.*401A=	ENSP00000423530.1:n.*401A=
ENST00000513688.1:n.608A=
NM_001278731.1:c.526A=	NP_001265660.1:p.Ser176=
NM_001278732.1:c.169A=	NP_001265661.1:p.Ser57=
NM_012208.3:c.601A=	NP_036340.1:p.Ser201=
XM_011537619.1:c.619A=	XP_011535921.1:p.Ser207=
XM_011537620.1:c.619A=	XP_011535922.1:p.Ser207=
NM_001363535.1:c.619A=	NP_001350464.1:p.Ser207=
NM_001363536.1:c.391A=	NP_001350465.1:p.Ser131=
XM_017009288.1:c.391A=	XP_016864777.1:p.Ser131=
XM_017009289.1:c.391A=	XP_016864778.1:p.Ser131=
XM_017009290.2:c.-134A=	XP_016864779.1:n.-134A=
XM_017009291.1:c.-134A=	XP_016864780.1:n.-134A=
XM_017009292.1:c.-134A=	XP_016864781.1:n.-134A=
NM_012208.4:c.601A= MANE Select	NP_036340.1:p.Ser201=
NM_001278731.2:c.526A=	NP_001265660.1:p.Ser176=
NM_001278732.2:c.169A=	NP_001265661.1:p.Ser57=
NM_001363535.2:c.619A=	NP_001350464.1:p.Ser207=
NM_001363536.2:c.391A=	NP_001350465.1:p.Ser131=