Canonical Allele Identifier: CA361198111

Gene: HARS2

Linked Data

• MyVariant Identifiers: chr5:g.140075359C>A (hg19) ; chr5:g.140695774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695774C>A , CM000667.2:g.140695774C>A	GRCh38
NC_000005.9:g.140075359C>A , CM000667.1:g.140075359C>A	GRCh37
NC_000005.8:g.140055543C>A	NCBI36
NG_021415.1:g.9342C>A
NG_032158.1:g.613G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.562C>A MANE Select	ENSP00000230771.3:p.Pro188Thr
ENST00000503873.6:c.340C>A	ENSP00000424516.2:p.Pro114Thr
ENST00000509299.6:c.352C>A	ENSP00000425695.2:p.Pro118Thr
ENST00000520095.6:c.*140C>A	ENSP00000429220.1:n.*140C>A
ENST00000642452.1:c.528C>A
ENST00000642752.1:c.562C>A	ENSP00000493630.1:p.Pro188Thr
ENST00000642970.1:c.352C>A	ENSP00000496011.1:p.Pro118Thr
ENST00000643996.1:c.352C>A	ENSP00000495350.1:p.Pro118Thr
ENST00000645065.1:c.580C>A	ENSP00000493571.1:p.Pro194Thr
ENST00000645749.1:c.562C>A	ENSP00000494296.1:p.Pro188Thr
ENST00000646468.1:c.580C>A	ENSP00000494965.1:p.Pro194Thr
ENST00000647484.1:c.352C>A	ENSP00000494140.1:p.Pro118Thr
ENST00000230771.7:c.562C>A	ENSP00000230771.3:p.Pro188Thr
ENST00000448069.2:c.145C>A	ENSP00000407105.2:p.Pro49Thr
ENST00000508522.5:c.487C>A	ENSP00000423616.1:p.Pro163Thr
ENST00000510104.5:c.*362C>A	ENSP00000423530.1:n.*362C>A
ENST00000513688.1:n.569C>A
NM_001278731.1:c.487C>A	NP_001265660.1:p.Pro163Thr
NM_001278732.1:c.130C>A	NP_001265661.1:p.Pro44Thr
NM_012208.3:c.562C>A	NP_036340.1:p.Pro188Thr
XM_011537619.1:c.580C>A	XP_011535921.1:p.Pro194Thr
XM_011537620.1:c.580C>A	XP_011535922.1:p.Pro194Thr
NM_001363535.1:c.580C>A	NP_001350464.1:p.Pro194Thr
NM_001363536.1:c.352C>A	NP_001350465.1:p.Pro118Thr
XM_017009288.1:c.352C>A	XP_016864777.1:p.Pro118Thr
XM_017009289.1:c.352C>A	XP_016864778.1:p.Pro118Thr
XM_017009290.2:c.-173C>A	XP_016864779.1:n.-173C>A
XM_017009291.1:c.-173C>A	XP_016864780.1:n.-173C>A
XM_017009292.1:c.-173C>A	XP_016864781.1:n.-173C>A
NM_012208.4:c.562C>A MANE Select	NP_036340.1:p.Pro188Thr
NM_001278731.2:c.487C>A	NP_001265660.1:p.Pro163Thr
NM_001278732.2:c.130C>A	NP_001265661.1:p.Pro44Thr
NM_001363535.2:c.580C>A	NP_001350464.1:p.Pro194Thr
NM_001363536.2:c.352C>A	NP_001350465.1:p.Pro118Thr