Canonical Allele Identifier: CA319185481

Gene: LTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28971391C>T , CM000683.2:g.28971391C>T	GRCh38
NC_000021.8:g.30343713C>T , CM000683.1:g.30343713C>T	GRCh37
NC_000021.7:g.29265584C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361371.10:c.864G>A MANE Select	ENSP00000354977.4:p.Gln288=
ENST00000389194.7:c.864G>A	ENSP00000373846.3:p.Gln288=
ENST00000389195.7:c.864G>A	ENSP00000373847.3:p.Gln288=
ENST00000361371.9:c.864G>A	ENSP00000354977.4:p.Gln288=
ENST00000389194.6:c.1002G>A	ENSP00000373846.2:p.Gln334=
ENST00000389195.6:c.1002G>A	ENSP00000373847.2:p.Gln334=
ENST00000483326.1:c.649G>A
ENST00000614971.4:c.1002G>A	ENSP00000478783.1:p.Gln334=
NM_015565.2:c.1002G>A	NP_056380.2:p.Gln334=
XM_006723987.2:c.1002G>A	XP_006724050.1:p.Gln334=
XM_011529525.1:c.1002G>A	XP_011527827.1:p.Gln334=
NM_001320766.2:c.864G>A	NP_001307695.2:p.Gln288=
NM_015565.3:c.864G>A MANE Select	NP_056380.3:p.Gln288=
XM_006723987.4:c.1002G>A	XP_006724050.1:p.Gln334=
XM_017028316.2:c.-4G>A	XP_016883805.1:n.-4G>A