Canonical Allele Identifier: CA1588995760

Gene: LARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146145585T>A , CM000667.2:g.146145585T>A	GRCh38
NC_000005.9:g.145525148T>A , CM000667.1:g.145525148T>A	GRCh37
NC_000005.8:g.145505341T>A	NCBI36
NG_042294.1:g.42147A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394434.7:c.1504-876A>T MANE Select	ENSP00000377954.2:n.1504-876A>T
ENST00000504323.6:n.972A>T
ENST00000506231.6:n.776A>T
ENST00000512412.2:n.1681-876A>T
ENST00000674158.1:c.1123-876A>T	ENSP00000501474.1:n.1123-876A>T
ENST00000674170.1:c.1574-876A>T	ENSP00000501381.1:n.1574-876A>T
ENST00000674174.1:c.1342-876A>T	ENSP00000501434.1:n.1342-876A>T
ENST00000674191.1:c.1048-876A>T	ENSP00000501478.1:n.1048-876A>T
ENST00000674218.1:n.1681-876A>T
ENST00000674270.1:c.1366-876A>T	ENSP00000501365.1:n.1366-876A>T
ENST00000674277.1:c.1342-876A>T	ENSP00000501510.1:n.1342-876A>T
ENST00000674290.1:c.1468-876A>T	ENSP00000501435.1:n.1468-876A>T
ENST00000674309.1:c.1504-876A>T	ENSP00000501400.1:n.1504-876A>T
ENST00000674310.1:c.1504-876A>T	ENSP00000501486.1:n.1504-876A>T
ENST00000674383.1:n.1547-876A>T
ENST00000674398.1:c.1504-876A>T	ENSP00000501476.1:n.1504-876A>T
ENST00000674447.1:c.1423-876A>T	ENSP00000501376.1:n.1423-876A>T
ENST00000674467.1:c.1504-876A>T	ENSP00000501351.1:n.1504-876A>T
ENST00000674471.1:n.688A>T
ENST00000674479.1:n.1681-876A>T
ENST00000274562.13:c.-102-2595A>T	ENSP00000274562.10:n.-102-2595A>T
ENST00000394434.6:c.1504-876A>T	ENSP00000377954.2:n.1504-876A>T
ENST00000507095.1:n.125-876A>T
ENST00000508667.5:n.166-876A>T
ENST00000510191.5:c.1342-876A>T	ENSP00000426005.1:n.1342-876A>T
NM_020117.9:c.1504-876A>T	NP_064502.9:n.1504-876A>T
XM_011537655.1:c.1366-876A>T	XP_011535957.1:n.1366-876A>T
XM_011537656.1:c.1342-876A>T	XP_011535958.1:n.1342-876A>T
XM_011537657.1:c.1504-876A>T	XP_011535959.1:n.1504-876A>T
NM_001317964.1:c.1366-876A>T	NP_001304893.1:n.1366-876A>T
NM_001317965.1:c.1342-876A>T	NP_001304894.1:n.1342-876A>T
NM_016460.3:c.1423-876A>T	NP_057544.2:n.1423-876A>T
NM_020117.10:c.1504-876A>T	NP_064502.9:n.1504-876A>T
XM_011537656.3:c.1342-876A>T	XP_011535958.1:n.1342-876A>T
NM_020117.11:c.1504-876A>T MANE Select	NP_064502.9:n.1504-876A>T
NM_001317964.2:c.1366-876A>T	NP_001304893.1:n.1366-876A>T
NM_001317965.2:c.1342-876A>T	NP_001304894.1:n.1342-876A>T
NM_016460.4:c.1423-876A>T	NP_057544.2:n.1423-876A>T