Canonical Allele Identifier: CA1586866731
Gene: HARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140695738G= , CM000667.2:g.140695738G= GRCh38
NC_000005.9:g.140075323G= , CM000667.1:g.140075323G= GRCh37
NC_000005.8:g.140055507G= NCBI36
NG_021415.1:g.9306G=
NG_032158.1:g.649C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230771.9:c.526G= MANE Select ENSP00000230771.3:p.Asp176=
ENST00000503873.6:c.304G= ENSP00000424516.2:p.Asp102=
ENST00000509299.6:c.316G= ENSP00000425695.2:p.Asp106=
ENST00000520095.6:c.*104G= ENSP00000429220.1:n.*104G=
ENST00000642452.1:c.492G=
ENST00000642752.1:c.526G= ENSP00000493630.1:p.Asp176=
ENST00000642970.1:c.316G= ENSP00000496011.1:p.Asp106=
ENST00000643996.1:c.316G= ENSP00000495350.1:p.Asp106=
ENST00000645065.1:c.544G= ENSP00000493571.1:p.Asp182=
ENST00000645749.1:c.526G= ENSP00000494296.1:p.Asp176=
ENST00000646468.1:c.544G= ENSP00000494965.1:p.Asp182=
ENST00000647484.1:c.316G= ENSP00000494140.1:p.Asp106=
ENST00000230771.7:c.526G= ENSP00000230771.3:p.Asp176=
ENST00000448069.2:c.109G= ENSP00000407105.2:p.Asp37=
ENST00000508522.5:c.451G= ENSP00000423616.1:p.Asp151=
ENST00000510104.5:c.*326G= ENSP00000423530.1:n.*326G=
ENST00000513688.1:n.533G=
ENST00000520095.5:c.*104G= ENSP00000429220.1:n.*104G=
NM_001278731.1:c.451G= NP_001265660.1:p.Asp151=
NM_001278732.1:c.94G= NP_001265661.1:p.Asp32=
NM_012208.3:c.526G= NP_036340.1:p.Asp176=
XM_011537619.1:c.544G= XP_011535921.1:p.Asp182=
XM_011537620.1:c.544G= XP_011535922.1:p.Asp182=
NM_001363535.1:c.544G= NP_001350464.1:p.Asp182=
NM_001363536.1:c.316G= NP_001350465.1:p.Asp106=
XM_017009288.1:c.316G= XP_016864777.1:p.Asp106=
XM_017009289.1:c.316G= XP_016864778.1:p.Asp106=
XM_017009290.2:c.-209G= XP_016864779.1:n.-209G=
XM_017009291.1:c.-209G= XP_016864780.1:n.-209G=
XM_017009292.1:c.-209G= XP_016864781.1:n.-209G=
NM_012208.4:c.526G= MANE Select NP_036340.1:p.Asp176=
NM_001278731.2:c.451G= NP_001265660.1:p.Asp151=
NM_001278732.2:c.94G= NP_001265661.1:p.Asp32=
NM_001363535.2:c.544G= NP_001350464.1:p.Asp182=
NM_001363536.2:c.316G= NP_001350465.1:p.Asp106=