Canonical Allele Identifier: CA1361691373
Gene: LARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45476510_45476514delinsGCCAC , CM000665.2:g.45476510_45476514delinsGCCAC GRCh38
NC_000003.11:g.45518002_45518006delinsGCCAC , CM000665.1:g.45518002_45518006delinsGCCAC GRCh37
NC_000003.10:g.45493006_45493010delinsGCCAC NCBI36
NG_033907.1:g.92928_92932delinsGCCAC
NG_033907.2:g.92928_92932delinsGCCAC
NG_033907.3:g.92947_92951delinsGCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265537.8:c.901_905delinsGCCAC ENSP00000265537.4:p.Ala301=
ENST00000642274.1:c.901_905delinsGCCAC ENSP00000495707.1:p.Ala301=
ENST00000645846.2:c.901_905delinsGCCAC MANE Select ENSP00000495093.1:p.Ala301=
ENST00000650792.2:c.901_905delinsGCCAC ENSP00000498867.1:p.Ala301=
ENST00000651549.1:c.901_905delinsGCCAC ENSP00000499002.1:p.Ala301=
ENST00000652135.1:c.*769_*773delinsGCCAC ENSP00000499104.1:n.*769_*773delinsGCCAC
ENST00000265537.7:c.901_905delinsGCCAC ENSP00000265537.3:p.Ala301=
ENST00000414984.5:c.772_776delinsGCCAC ENSP00000412893.1:p.Ala258=
ENST00000415258.5:c.901_905delinsGCCAC ENSP00000408576.1:p.Ala301=
NM_015340.3:c.901_905delinsGCCAC NP_056155.1:p.Ala301=
XM_005265006.1:c.901_905delinsGCCAC XP_005265063.1:p.Ala301=
XM_011533554.1:c.901_905delinsGCCAC XP_011531856.1:p.Ala301=
XM_005265006.2:c.901_905delinsGCCAC XP_005265063.1:p.Ala301=
XM_011533554.2:c.901_905delinsGCCAC XP_011531856.1:p.Ala301=
XM_017006042.1:c.901_905delinsGCCAC XP_016861531.1:p.Ala301=
NM_015340.4:c.901_905delinsGCCAC MANE Select NP_056155.1:p.Ala301=
NM_001368263.1:c.901_905delinsGCCAC NP_001355192.1:p.Ala301=