Canonical Allele Identifier: CA1361703937

Gene: LARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45516144G= , CM000665.2:g.45516144G=	GRCh38
NC_000003.11:g.45557636G= , CM000665.1:g.45557636G=	GRCh37
NC_000003.10:g.45532640G=	NCBI36
NG_033907.1:g.132562G=
NG_033907.2:g.132562G=
NG_033907.3:g.132581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265537.8:c.*302G=	ENSP00000265537.4:n.*302G=
ENST00000642274.1:c.1912G=	ENSP00000495707.1:p.Glu638=
ENST00000645846.2:c.1912G= MANE Select	ENSP00000495093.1:p.Glu638=
ENST00000650792.2:c.1912G=	ENSP00000498867.1:p.Glu638=
ENST00000651549.1:c.*202G=	ENSP00000499002.1:n.*202G=
ENST00000652135.1:c.*1780G=	ENSP00000499104.1:n.*1780G=
ENST00000265537.7:c.1912G=	ENSP00000265537.3:p.Glu638=
ENST00000414984.5:c.1783G=	ENSP00000412893.1:p.Glu595=
ENST00000415258.5:c.1912G=	ENSP00000408576.1:p.Glu638=
ENST00000467936.5:n.191G=
NM_015340.3:c.1912G=	NP_056155.1:p.Glu638=
XM_005265006.1:c.1912G=	XP_005265063.1:p.Glu638=
XM_011533554.1:c.1912G=	XP_011531856.1:p.Glu638=
XM_005265006.2:c.1912G=	XP_005265063.1:p.Glu638=
XM_011533554.2:c.1912G=	XP_011531856.1:p.Glu638=
XM_017006042.1:c.1912G=	XP_016861531.1:p.Glu638=
NM_015340.4:c.1912G= MANE Select	NP_056155.1:p.Glu638=
NM_001368263.1:c.1912G=	NP_001355192.1:p.Glu638=