Canonical Allele Identifier: CA1361675964

Gene: LARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45435202G= , CM000665.2:g.45435202G=	GRCh38
NC_000003.11:g.45476694G= , CM000665.1:g.45476694G=	GRCh37
NC_000003.10:g.45451698G=	NCBI36
NG_033907.1:g.51620G=
NG_033907.2:g.51620G=
NG_033907.3:g.51639G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015340.4:c.517-11689G= MANE Select	NP_056155.1:n.517-11689G=
ENST00000645846.2:c.517-11689G= MANE Select	ENSP00000495093.1:n.517-11689G=
NM_001368263.1:c.517-11689G=	NP_001355192.1:n.517-11689G=
NM_015340.3:c.517-11689G=	NP_056155.1:n.517-11689G=
ENST00000265537.7:c.517-11689G=	ENSP00000265537.3:n.517-11689G=
ENST00000265537.8:c.517-11689G=	ENSP00000265537.4:n.517-11689G=
ENST00000414984.5:c.388-11689G=	ENSP00000412893.1:n.388-11689G=
ENST00000415258.5:c.517-11689G=	ENSP00000408576.1:n.517-11689G=
ENST00000431023.5:c.388-11689G=	ENSP00000406611.1:n.388-11689G=
ENST00000642274.1:c.517-11689G=	ENSP00000495707.1:n.517-11689G=
ENST00000650792.2:c.517-11689G=	ENSP00000498867.1:n.517-11689G=
ENST00000651549.1:c.517-11689G=	ENSP00000499002.1:n.517-11689G=
ENST00000652135.1:c.*385-11689G=	ENSP00000499104.1:n.*385-11689G=
XM_005265006.1:c.517-11689G=	XP_005265063.1:n.517-11689G=
XM_005265006.2:c.517-11689G=	XP_005265063.1:n.517-11689G=
XM_011533554.1:c.517-11689G=	XP_011531856.1:n.517-11689G=
XM_011533554.2:c.517-11689G=	XP_011531856.1:n.517-11689G=
XM_017006042.1:c.517-11689G=	XP_016861531.1:n.517-11689G=