Canonical Allele Identifier: CA1361691375

Gene: LARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45476513_45476514delinsAC , CM000665.2:g.45476513_45476514delinsAC	GRCh38
NC_000003.11:g.45518005_45518006delinsAC , CM000665.1:g.45518005_45518006delinsAC	GRCh37
NC_000003.10:g.45493009_45493010delinsAC	NCBI36
NG_033907.1:g.92931_92932delinsAC
NG_033907.2:g.92931_92932delinsAC
NG_033907.3:g.92950_92951delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265537.8:c.904_905delinsAC	ENSP00000265537.4:p.Thr302=
ENST00000642274.1:c.904_905delinsAC	ENSP00000495707.1:p.Thr302=
ENST00000645846.2:c.904_905delinsAC MANE Select	ENSP00000495093.1:p.Thr302=
ENST00000650792.2:c.904_905delinsAC	ENSP00000498867.1:p.Thr302=
ENST00000651549.1:c.904_905delinsAC	ENSP00000499002.1:p.Thr302=
ENST00000652135.1:c.*772_*773delinsAC	ENSP00000499104.1:n.*772_*773delinsAC
ENST00000265537.7:c.904_905delinsAC	ENSP00000265537.3:p.Thr302=
ENST00000414984.5:c.775_776delinsAC	ENSP00000412893.1:p.Thr259=
ENST00000415258.5:c.904_905delinsAC	ENSP00000408576.1:p.Thr302=
NM_015340.3:c.904_905delinsAC	NP_056155.1:p.Thr302=
XM_005265006.1:c.904_905delinsAC	XP_005265063.1:p.Thr302=
XM_011533554.1:c.904_905delinsAC	XP_011531856.1:p.Thr302=
XM_005265006.2:c.904_905delinsAC	XP_005265063.1:p.Thr302=
XM_011533554.2:c.904_905delinsAC	XP_011531856.1:p.Thr302=
XM_017006042.1:c.904_905delinsAC	XP_016861531.1:p.Thr302=
NM_015340.4:c.904_905delinsAC MANE Select	NP_056155.1:p.Thr302=
NM_001368263.1:c.904_905delinsAC	NP_001355192.1:p.Thr302=