Canonical Allele Identifier: CA2665386322

Gene: LARS2

Linked Data

• gnomAD v4: 3-45476601-TGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45476604_45476606del , CM000665.2:g.45476604_45476606del	GRCh38
NC_000003.11:g.45518096_45518098del , CM000665.1:g.45518096_45518098del	GRCh37
NC_000003.10:g.45493100_45493102del	NCBI36
NG_033907.1:g.93022_93024del
NG_033907.2:g.93022_93024del
NG_033907.3:g.93041_93043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265537.8:c.995_997del	ENSP00000265537.4:p.Arg332del
ENST00000642274.1:c.995_997del	ENSP00000495707.1:p.Arg332del
ENST00000645846.2:c.995_997del MANE Select	ENSP00000495093.1:p.Arg332del
ENST00000650792.2:c.995_997del	ENSP00000498867.1:p.Arg332del
ENST00000651549.1:c.995_997del	ENSP00000499002.1:p.Arg332del
ENST00000652135.1:c.*863_*865del	ENSP00000499104.1:n.*863_*865del
ENST00000265537.7:c.995_997del	ENSP00000265537.3:p.Arg332del
ENST00000414984.5:c.866_868del	ENSP00000412893.1:p.Arg289del
ENST00000415258.5:c.995_997del	ENSP00000408576.1:p.Arg332del
NM_015340.3:c.995_997del	NP_056155.1:p.Arg332del
XM_005265006.1:c.995_997del	XP_005265063.1:p.Arg332del
XM_011533554.1:c.995_997del	XP_011531856.1:p.Arg332del
XM_005265006.2:c.995_997del	XP_005265063.1:p.Arg332del
XM_011533554.2:c.995_997del	XP_011531856.1:p.Arg332del
XM_017006042.1:c.995_997del	XP_016861531.1:p.Arg332del
NM_015340.4:c.995_997del MANE Select	NP_056155.1:p.Arg332del
NM_001368263.1:c.995_997del	NP_001355192.1:p.Arg332del