Canonical Allele Identifier: CA1361658552
Gene: LARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45399229A= , CM000665.2:g.45399229A= GRCh38
NC_000003.11:g.45440721A= , CM000665.1:g.45440721A= GRCh37
NC_000003.10:g.45415725A= NCBI36
NG_033907.1:g.15647A=
NG_033907.2:g.15647A=
NG_033907.3:g.15666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265537.8:c.235-1016A= ENSP00000265537.4:n.235-1016A=
ENST00000431023.6:n.361-1016A=
ENST00000642274.1:c.235-1016A= ENSP00000495707.1:n.235-1016A=
ENST00000645846.2:c.235-1016A= MANE Select ENSP00000495093.1:n.235-1016A=
ENST00000650792.2:c.235-1016A= ENSP00000498867.1:n.235-1016A=
ENST00000651549.1:c.235-1016A= ENSP00000499002.1:n.235-1016A=
ENST00000652135.1:c.235-335A= ENSP00000499104.1:n.235-335A=
ENST00000265537.7:c.235-1016A= ENSP00000265537.3:n.235-1016A=
ENST00000414984.5:c.234+4542A= ENSP00000412893.1:n.234+4542A=
ENST00000415258.5:c.235-1016A= ENSP00000408576.1:n.235-1016A=
ENST00000430399.1:c.235-1016A= ENSP00000401388.1:n.235-1016A=
ENST00000431023.5:c.234+4542A= ENSP00000406611.1:n.234+4542A=
NM_015340.3:c.235-1016A= NP_056155.1:n.235-1016A=
XM_005265006.1:c.235-1016A= XP_005265063.1:n.235-1016A=
XM_011533554.1:c.235-1016A= XP_011531856.1:n.235-1016A=
XM_005265006.2:c.235-1016A= XP_005265063.1:n.235-1016A=
XM_011533554.2:c.235-1016A= XP_011531856.1:n.235-1016A=
XM_017006042.1:c.235-1016A= XP_016861531.1:n.235-1016A=
NM_015340.4:c.235-1016A= MANE Select NP_056155.1:n.235-1016A=
NM_001368263.1:c.235-1016A= NP_001355192.1:n.235-1016A=