Canonical Allele Identifier: CA1361691445

Gene: LARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45476667A= , CM000665.2:g.45476667A=	GRCh38
NC_000003.11:g.45518159A= , CM000665.1:g.45518159A=	GRCh37
NC_000003.10:g.45493163A=	NCBI36
NG_033907.1:g.93085A=
NG_033907.2:g.93085A=
NG_033907.3:g.93104A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265537.8:c.1018+40A=	ENSP00000265537.4:n.1018+40A=
ENST00000642274.1:c.1018+40A=	ENSP00000495707.1:n.1018+40A=
ENST00000645846.2:c.1018+40A= MANE Select	ENSP00000495093.1:n.1018+40A=
ENST00000650792.2:c.1018+40A=	ENSP00000498867.1:n.1018+40A=
ENST00000651549.1:c.1018+40A=	ENSP00000499002.1:n.1018+40A=
ENST00000652135.1:c.*886+40A=	ENSP00000499104.1:n.*886+40A=
ENST00000265537.7:c.1018+40A=	ENSP00000265537.3:n.1018+40A=
ENST00000414984.5:c.889+40A=	ENSP00000412893.1:n.889+40A=
ENST00000415258.5:c.1018+40A=	ENSP00000408576.1:n.1018+40A=
NM_015340.3:c.1018+40A=	NP_056155.1:n.1018+40A=
XM_005265006.1:c.1018+40A=	XP_005265063.1:n.1018+40A=
XM_011533554.1:c.1018+40A=	XP_011531856.1:n.1018+40A=
XM_005265006.2:c.1018+40A=	XP_005265063.1:n.1018+40A=
XM_011533554.2:c.1018+40A=	XP_011531856.1:n.1018+40A=
XM_017006042.1:c.1018+40A=	XP_016861531.1:n.1018+40A=
NM_015340.4:c.1018+40A= MANE Select	NP_056155.1:n.1018+40A=
NM_001368263.1:c.1018+40A=	NP_001355192.1:n.1018+40A=