Canonical Allele Identifier: CA1586869543

Gene: HARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140697311G= , CM000667.2:g.140697311G=	GRCh38
NC_000005.9:g.140076896G= , CM000667.1:g.140076896G=	GRCh37
NC_000005.8:g.140057080G=	NCBI36
NG_021415.1:g.10879G=

Transcript Alleles

HGVS	Amino-acid Change
NM_012208.4:c.1102G= MANE Select	NP_036340.1:p.Val368=
ENST00000230771.9:c.1102G= MANE Select	ENSP00000230771.3:p.Val368=
NM_001278731.1:c.1027G=	NP_001265660.1:p.Val343=
NM_001278731.2:c.1027G=	NP_001265660.1:p.Val343=
NM_001278732.1:c.670G=	NP_001265661.1:p.Val224=
NM_001278732.2:c.670G=	NP_001265661.1:p.Val224=
NM_001363535.1:c.1120G=	NP_001350464.1:p.Val374=
NM_001363535.2:c.1120G=	NP_001350464.1:p.Val374=
NM_001363536.1:c.892G=	NP_001350465.1:p.Val298=
NM_001363536.2:c.892G=	NP_001350465.1:p.Val298=
NM_012208.3:c.1102G=	NP_036340.1:p.Val368=
ENST00000230771.7:c.1102G=	ENSP00000230771.3:p.Val368=
ENST00000448069.2:c.586G=	ENSP00000407105.2:p.Val196=
ENST00000503873.6:c.781G=	ENSP00000424516.2:p.Val261=
ENST00000508522.5:c.1027G=	ENSP00000423616.1:p.Val343=
ENST00000520095.6:c.*680G=	ENSP00000429220.1:n.*680G=
ENST00000642452.1:c.1142G=
ENST00000642752.1:c.1003G=	ENSP00000493630.1:p.Val335=
ENST00000642970.1:c.892G=	ENSP00000496011.1:p.Val298=
ENST00000643996.1:c.892G=	ENSP00000495350.1:p.Val298=
ENST00000645065.1:c.1120G=	ENSP00000493571.1:p.Val374=
ENST00000645749.1:c.1102G=	ENSP00000494296.1:p.Val368=
ENST00000646468.1:c.1120G=	ENSP00000494965.1:p.Val374=
ENST00000647484.1:c.*483G=	ENSP00000494140.1:n.*483G=
XM_011537619.1:c.1120G=	XP_011535921.1:p.Val374=
XM_011537620.1:c.1021G=	XP_011535922.1:p.Val341=
XM_017009288.1:c.892G=	XP_016864777.1:p.Val298=
XM_017009289.1:c.892G=	XP_016864778.1:p.Val298=
XM_017009290.2:c.442G=	XP_016864779.1:p.Val148=
XM_017009291.1:c.442G=	XP_016864780.1:p.Val148=
XM_017009292.1:c.442G=	XP_016864781.1:p.Val148=