Canonical Allele Identifier: CA446804440

Gene: HARS2

Linked Data

• MyVariant Identifiers: chr5:g.140075406G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695821G>A , CM000667.2:g.140695821G>A	GRCh38
NC_000005.9:g.140075406G>A , CM000667.1:g.140075406G>A	GRCh37
NC_000005.8:g.140055590G>A	NCBI36
NG_021415.1:g.9389G>A
NG_032158.1:g.566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.609G>A MANE Select	ENSP00000230771.3:p.Leu203=
ENST00000503873.6:c.387G>A	ENSP00000424516.2:p.Leu129=
ENST00000509299.6:c.399G>A	ENSP00000425695.2:p.Leu133=
ENST00000520095.6:c.*187G>A	ENSP00000429220.1:n.*187G>A
ENST00000642452.1:c.575G>A
ENST00000642752.1:c.609G>A	ENSP00000493630.1:p.Leu203=
ENST00000642970.1:c.399G>A	ENSP00000496011.1:p.Leu133=
ENST00000643996.1:c.399G>A	ENSP00000495350.1:p.Leu133=
ENST00000645065.1:c.627G>A	ENSP00000493571.1:p.Leu209=
ENST00000645749.1:c.609G>A	ENSP00000494296.1:p.Leu203=
ENST00000646468.1:c.627G>A	ENSP00000494965.1:p.Leu209=
ENST00000647484.1:c.399G>A	ENSP00000494140.1:p.Leu133=
ENST00000230771.7:c.609G>A	ENSP00000230771.3:p.Leu203=
ENST00000448069.2:c.192G>A	ENSP00000407105.2:p.Leu64=
ENST00000508522.5:c.534G>A	ENSP00000423616.1:p.Leu178=
ENST00000510104.5:c.*409G>A	ENSP00000423530.1:n.*409G>A
ENST00000513688.1:n.616G>A
NM_001278731.1:c.534G>A	NP_001265660.1:p.Leu178=
NM_001278732.1:c.177G>A	NP_001265661.1:p.Leu59=
NM_012208.3:c.609G>A	NP_036340.1:p.Leu203=
XM_011537619.1:c.627G>A	XP_011535921.1:p.Leu209=
XM_011537620.1:c.627G>A	XP_011535922.1:p.Leu209=
NM_001363535.1:c.627G>A	NP_001350464.1:p.Leu209=
NM_001363536.1:c.399G>A	NP_001350465.1:p.Leu133=
XM_017009288.1:c.399G>A	XP_016864777.1:p.Leu133=
XM_017009289.1:c.399G>A	XP_016864778.1:p.Leu133=
XM_017009290.2:c.-126G>A	XP_016864779.1:n.-126G>A
XM_017009291.1:c.-126G>A	XP_016864780.1:n.-126G>A
XM_017009292.1:c.-126G>A	XP_016864781.1:n.-126G>A
NM_012208.4:c.609G>A MANE Select	NP_036340.1:p.Leu203=
NM_001278731.2:c.534G>A	NP_001265660.1:p.Leu178=
NM_001278732.2:c.177G>A	NP_001265661.1:p.Leu59=
NM_001363535.2:c.627G>A	NP_001350464.1:p.Leu209=
NM_001363536.2:c.399G>A	NP_001350465.1:p.Leu133=