Canonical Allele Identifier: CA361196966

Gene: HARS2

Linked Data

• MyVariant Identifiers: chr5:g.140075094T>C (hg19) ; chr5:g.140695509T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140695509T>C , CM000667.2:g.140695509T>C	GRCh38
NC_000005.9:g.140075094T>C , CM000667.1:g.140075094T>C	GRCh37
NC_000005.8:g.140055278T>C	NCBI36
NG_021415.1:g.9077T>C
NG_032158.1:g.878A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230771.9:c.401T>C MANE Select	ENSP00000230771.3:p.Val134Ala
ENST00000503873.6:c.304-229T>C	ENSP00000424516.2:n.304-229T>C
ENST00000509299.6:c.191T>C	ENSP00000425695.2:p.Val64Ala
ENST00000520095.6:c.*104-229T>C	ENSP00000429220.1:n.*104-229T>C
ENST00000642452.1:c.367T>C
ENST00000642752.1:c.401T>C	ENSP00000493630.1:p.Val134Ala
ENST00000642970.1:c.191T>C	ENSP00000496011.1:p.Val64Ala
ENST00000643996.1:c.191T>C	ENSP00000495350.1:p.Val64Ala
ENST00000645065.1:c.419T>C	ENSP00000493571.1:p.Val140Ala
ENST00000645749.1:c.401T>C	ENSP00000494296.1:p.Val134Ala
ENST00000646468.1:c.419T>C	ENSP00000494965.1:p.Val140Ala
ENST00000647484.1:c.191T>C	ENSP00000494140.1:p.Val64Ala
ENST00000230771.7:c.401T>C	ENSP00000230771.3:p.Val134Ala
ENST00000448069.2:c.109-229T>C	ENSP00000407105.2:n.109-229T>C
ENST00000502303.5:n.484T>C
ENST00000508522.5:c.326T>C	ENSP00000423616.1:p.Val109Ala
ENST00000509299.5:c.419T>C	ENSP00000425695.1:p.Val140Ala
ENST00000510104.5:c.*201T>C	ENSP00000423530.1:n.*201T>C
ENST00000513688.1:n.408T>C
ENST00000520095.5:c.*104-229T>C	ENSP00000429220.1:n.*104-229T>C
NM_001278731.1:c.326T>C	NP_001265660.1:p.Val109Ala
NM_001278732.1:c.94-229T>C	NP_001265661.1:n.94-229T>C
NM_012208.3:c.401T>C	NP_036340.1:p.Val134Ala
XM_011537619.1:c.419T>C	XP_011535921.1:p.Val140Ala
XM_011537620.1:c.419T>C	XP_011535922.1:p.Val140Ala
NM_001363535.1:c.419T>C	NP_001350464.1:p.Val140Ala
NM_001363536.1:c.191T>C	NP_001350465.1:p.Val64Ala
XM_017009288.1:c.191T>C	XP_016864777.1:p.Val64Ala
XM_017009289.1:c.191T>C	XP_016864778.1:p.Val64Ala
XM_017009290.2:c.-334T>C	XP_016864779.1:n.-334T>C
XM_017009291.1:c.-334T>C	XP_016864780.1:n.-334T>C
XM_017009292.1:c.-334T>C	XP_016864781.1:n.-334T>C
NM_012208.4:c.401T>C MANE Select	NP_036340.1:p.Val134Ala
NM_001278731.2:c.326T>C	NP_001265660.1:p.Val109Ala
NM_001278732.2:c.94-229T>C	NP_001265661.1:n.94-229T>C
NM_001363535.2:c.419T>C	NP_001350464.1:p.Val140Ala
NM_001363536.2:c.191T>C	NP_001350465.1:p.Val64Ala