Canonical Allele Identifier: CA361197444
Gene: HARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140695578G>C , CM000667.2:g.140695578G>C GRCh38
NC_000005.9:g.140075163G>C , CM000667.1:g.140075163G>C GRCh37
NC_000005.8:g.140055347G>C NCBI36
NG_021415.1:g.9146G>C
NG_032158.1:g.809C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230771.9:c.470G>C MANE Select ENSP00000230771.3:p.Trp157Ser
ENST00000503873.6:c.304-160G>C ENSP00000424516.2:n.304-160G>C
ENST00000509299.6:c.260G>C ENSP00000425695.2:p.Trp87Ser
ENST00000520095.6:c.*104-160G>C ENSP00000429220.1:n.*104-160G>C
ENST00000642452.1:c.436G>C
ENST00000642752.1:c.470G>C ENSP00000493630.1:p.Trp157Ser
ENST00000642970.1:c.260G>C ENSP00000496011.1:p.Trp87Ser
ENST00000643996.1:c.260G>C ENSP00000495350.1:p.Trp87Ser
ENST00000645065.1:c.488G>C ENSP00000493571.1:p.Trp163Ser
ENST00000645749.1:c.470G>C ENSP00000494296.1:p.Trp157Ser
ENST00000646468.1:c.488G>C ENSP00000494965.1:p.Trp163Ser
ENST00000647484.1:c.260G>C ENSP00000494140.1:p.Trp87Ser
ENST00000230771.7:c.470G>C ENSP00000230771.3:p.Trp157Ser
ENST00000448069.2:c.109-160G>C ENSP00000407105.2:n.109-160G>C
ENST00000508522.5:c.395G>C ENSP00000423616.1:p.Trp132Ser
ENST00000509299.5:c.488G>C ENSP00000425695.1:p.Trp163Ser
ENST00000510104.5:c.*270G>C ENSP00000423530.1:n.*270G>C
ENST00000513688.1:n.477G>C
ENST00000520095.5:c.*104-160G>C ENSP00000429220.1:n.*104-160G>C
NM_001278731.1:c.395G>C NP_001265660.1:p.Trp132Ser
NM_001278732.1:c.94-160G>C NP_001265661.1:n.94-160G>C
NM_012208.3:c.470G>C NP_036340.1:p.Trp157Ser
XM_011537619.1:c.488G>C XP_011535921.1:p.Trp163Ser
XM_011537620.1:c.488G>C XP_011535922.1:p.Trp163Ser
NM_001363535.1:c.488G>C NP_001350464.1:p.Trp163Ser
NM_001363536.1:c.260G>C NP_001350465.1:p.Trp87Ser
XM_017009288.1:c.260G>C XP_016864777.1:p.Trp87Ser
XM_017009289.1:c.260G>C XP_016864778.1:p.Trp87Ser
XM_017009290.2:c.-265G>C XP_016864779.1:n.-265G>C
XM_017009291.1:c.-265G>C XP_016864780.1:n.-265G>C
XM_017009292.1:c.-265G>C XP_016864781.1:n.-265G>C
NM_012208.4:c.470G>C MANE Select NP_036340.1:p.Trp157Ser
NM_001278731.2:c.395G>C NP_001265660.1:p.Trp132Ser
NM_001278732.2:c.94-160G>C NP_001265661.1:n.94-160G>C
NM_001363535.2:c.488G>C NP_001350464.1:p.Trp163Ser
NM_001363536.2:c.260G>C NP_001350465.1:p.Trp87Ser