Canonical Allele Identifier: CA1586866763
Gene: HARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140695755T= , CM000667.2:g.140695755T= GRCh38
NC_000005.9:g.140075340T= , CM000667.1:g.140075340T= GRCh37
NC_000005.8:g.140055524T= NCBI36
NG_021415.1:g.9323T=
NG_032158.1:g.632A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230771.9:c.543T= MANE Select ENSP00000230771.3:p.Gly181=
ENST00000503873.6:c.321T= ENSP00000424516.2:p.Gly107=
ENST00000509299.6:c.333T= ENSP00000425695.2:p.Gly111=
ENST00000520095.6:c.*121T= ENSP00000429220.1:n.*121T=
ENST00000642452.1:c.509T=
ENST00000642752.1:c.543T= ENSP00000493630.1:p.Gly181=
ENST00000642970.1:c.333T= ENSP00000496011.1:p.Gly111=
ENST00000643996.1:c.333T= ENSP00000495350.1:p.Gly111=
ENST00000645065.1:c.561T= ENSP00000493571.1:p.Gly187=
ENST00000645749.1:c.543T= ENSP00000494296.1:p.Gly181=
ENST00000646468.1:c.561T= ENSP00000494965.1:p.Gly187=
ENST00000647484.1:c.333T= ENSP00000494140.1:p.Gly111=
ENST00000230771.7:c.543T= ENSP00000230771.3:p.Gly181=
ENST00000448069.2:c.126T= ENSP00000407105.2:p.Gly42=
ENST00000508522.5:c.468T= ENSP00000423616.1:p.Gly156=
ENST00000510104.5:c.*343T= ENSP00000423530.1:n.*343T=
ENST00000513688.1:n.550T=
ENST00000520095.5:c.*121T= ENSP00000429220.1:n.*121T=
NM_001278731.1:c.468T= NP_001265660.1:p.Gly156=
NM_001278732.1:c.111T= NP_001265661.1:p.Gly37=
NM_012208.3:c.543T= NP_036340.1:p.Gly181=
XM_011537619.1:c.561T= XP_011535921.1:p.Gly187=
XM_011537620.1:c.561T= XP_011535922.1:p.Gly187=
NM_001363535.1:c.561T= NP_001350464.1:p.Gly187=
NM_001363536.1:c.333T= NP_001350465.1:p.Gly111=
XM_017009288.1:c.333T= XP_016864777.1:p.Gly111=
XM_017009289.1:c.333T= XP_016864778.1:p.Gly111=
XM_017009290.2:c.-192T= XP_016864779.1:n.-192T=
XM_017009291.1:c.-192T= XP_016864780.1:n.-192T=
XM_017009292.1:c.-192T= XP_016864781.1:n.-192T=
NM_012208.4:c.543T= MANE Select NP_036340.1:p.Gly181=
NM_001278731.2:c.468T= NP_001265660.1:p.Gly156=
NM_001278732.2:c.111T= NP_001265661.1:p.Gly37=
NM_001363535.2:c.561T= NP_001350464.1:p.Gly187=
NM_001363536.2:c.333T= NP_001350465.1:p.Gly111=