Canonical Allele Identifier: CA1361703892

Gene: LARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45516118C= , CM000665.2:g.45516118C=	GRCh38
NC_000003.11:g.45557610C= , CM000665.1:g.45557610C=	GRCh37
NC_000003.10:g.45532614C=	NCBI36
NG_033907.1:g.132536C=
NG_033907.2:g.132536C=
NG_033907.3:g.132555C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015340.4:c.1886C= MANE Select	NP_056155.1:p.Thr629=
ENST00000645846.2:c.1886C= MANE Select	ENSP00000495093.1:p.Thr629=
NM_001368263.1:c.1886C=	NP_001355192.1:p.Thr629=
NM_015340.3:c.1886C=	NP_056155.1:p.Thr629=
ENST00000265537.7:c.1886C=	ENSP00000265537.3:p.Thr629=
ENST00000265537.8:c.*276C=	ENSP00000265537.4:n.*276C=
ENST00000414984.5:c.1757C=	ENSP00000412893.1:p.Thr586=
ENST00000415258.5:c.1886C=	ENSP00000408576.1:p.Thr629=
ENST00000467936.5:n.165C=
ENST00000642274.1:c.1886C=	ENSP00000495707.1:p.Thr629=
ENST00000650792.2:c.1886C=	ENSP00000498867.1:p.Thr629=
ENST00000651549.1:c.*176C=	ENSP00000499002.1:n.*176C=
ENST00000652135.1:c.*1754C=	ENSP00000499104.1:n.*1754C=
XM_005265006.1:c.1886C=	XP_005265063.1:p.Thr629=
XM_005265006.2:c.1886C=	XP_005265063.1:p.Thr629=
XM_011533554.1:c.1886C=	XP_011531856.1:p.Thr629=
XM_011533554.2:c.1886C=	XP_011531856.1:p.Thr629=
XM_017006042.1:c.1886C=	XP_016861531.1:p.Thr629=