Canonical Allele Identifier: CA1361691411
Gene: LARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45476602G= , CM000665.2:g.45476602G= GRCh38
NC_000003.11:g.45518094G= , CM000665.1:g.45518094G= GRCh37
NC_000003.10:g.45493098G= NCBI36
NG_033907.1:g.93020G=
NG_033907.2:g.93020G=
NG_033907.3:g.93039G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265537.8:c.993G= ENSP00000265537.4:p.Leu331=
ENST00000642274.1:c.993G= ENSP00000495707.1:p.Leu331=
ENST00000645846.2:c.993G= MANE Select ENSP00000495093.1:p.Leu331=
ENST00000650792.2:c.993G= ENSP00000498867.1:p.Leu331=
ENST00000651549.1:c.993G= ENSP00000499002.1:p.Leu331=
ENST00000652135.1:c.*861G= ENSP00000499104.1:n.*861G=
ENST00000265537.7:c.993G= ENSP00000265537.3:p.Leu331=
ENST00000414984.5:c.864G= ENSP00000412893.1:p.Leu288=
ENST00000415258.5:c.993G= ENSP00000408576.1:p.Leu331=
NM_015340.3:c.993G= NP_056155.1:p.Leu331=
XM_005265006.1:c.993G= XP_005265063.1:p.Leu331=
XM_011533554.1:c.993G= XP_011531856.1:p.Leu331=
XM_005265006.2:c.993G= XP_005265063.1:p.Leu331=
XM_011533554.2:c.993G= XP_011531856.1:p.Leu331=
XM_017006042.1:c.993G= XP_016861531.1:p.Leu331=
NM_015340.4:c.993G= MANE Select NP_056155.1:p.Leu331=
NM_001368263.1:c.993G= NP_001355192.1:p.Leu331=