Canonical Allele Identifier: CA1586866804
Gene: HARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140695768A= , CM000667.2:g.140695768A= GRCh38
NC_000005.9:g.140075353A= , CM000667.1:g.140075353A= GRCh37
NC_000005.8:g.140055537A= NCBI36
NG_021415.1:g.9336A=
NG_032158.1:g.619T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230771.9:c.556A= MANE Select ENSP00000230771.3:p.Met186=
ENST00000503873.6:c.334A= ENSP00000424516.2:p.Met112=
ENST00000509299.6:c.346A= ENSP00000425695.2:p.Met116=
ENST00000520095.6:c.*134A= ENSP00000429220.1:n.*134A=
ENST00000642452.1:c.522A=
ENST00000642752.1:c.556A= ENSP00000493630.1:p.Met186=
ENST00000642970.1:c.346A= ENSP00000496011.1:p.Met116=
ENST00000643996.1:c.346A= ENSP00000495350.1:p.Met116=
ENST00000645065.1:c.574A= ENSP00000493571.1:p.Met192=
ENST00000645749.1:c.556A= ENSP00000494296.1:p.Met186=
ENST00000646468.1:c.574A= ENSP00000494965.1:p.Met192=
ENST00000647484.1:c.346A= ENSP00000494140.1:p.Met116=
ENST00000230771.7:c.556A= ENSP00000230771.3:p.Met186=
ENST00000448069.2:c.139A= ENSP00000407105.2:p.Met47=
ENST00000508522.5:c.481A= ENSP00000423616.1:p.Met161=
ENST00000510104.5:c.*356A= ENSP00000423530.1:n.*356A=
ENST00000513688.1:n.563A=
ENST00000520095.5:c.*134A= ENSP00000429220.1:n.*134A=
NM_001278731.1:c.481A= NP_001265660.1:p.Met161=
NM_001278732.1:c.124A= NP_001265661.1:p.Met42=
NM_012208.3:c.556A= NP_036340.1:p.Met186=
XM_011537619.1:c.574A= XP_011535921.1:p.Met192=
XM_011537620.1:c.574A= XP_011535922.1:p.Met192=
NM_001363535.1:c.574A= NP_001350464.1:p.Met192=
NM_001363536.1:c.346A= NP_001350465.1:p.Met116=
XM_017009288.1:c.346A= XP_016864777.1:p.Met116=
XM_017009289.1:c.346A= XP_016864778.1:p.Met116=
XM_017009290.2:c.-179A= XP_016864779.1:n.-179A=
XM_017009291.1:c.-179A= XP_016864780.1:n.-179A=
XM_017009292.1:c.-179A= XP_016864781.1:n.-179A=
NM_012208.4:c.556A= MANE Select NP_036340.1:p.Met186=
NM_001278731.2:c.481A= NP_001265660.1:p.Met161=
NM_001278732.2:c.124A= NP_001265661.1:p.Met42=
NM_001363535.2:c.574A= NP_001350464.1:p.Met192=
NM_001363536.2:c.346A= NP_001350465.1:p.Met116=