Canonical Allele Identifier: CA2085827

Gene: LANCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210472037G>T , CM000664.2:g.210472037G>T	GRCh38
NC_000002.11:g.211336761G>T , CM000664.1:g.211336761G>T	GRCh37
NC_000002.10:g.211045006G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448951.6:c.121C>A	ENSP00000396518.2:p.Arg41=
ENST00000450366.7:c.121C>A MANE Select	ENSP00000393597.2:p.Arg41=
ENST00000233714.8:c.121C>A	ENSP00000233714.4:p.Arg41=
ENST00000431941.6:c.121C>A	ENSP00000397646.2:p.Arg41=
ENST00000441020.7:c.121C>A	ENSP00000393323.3:p.Arg41=
ENST00000443314.5:c.121C>A	ENSP00000388713.1:p.Arg41=
ENST00000448951.5:c.121C>A	ENSP00000396518.1:p.Arg41=
ENST00000450366.6:c.121C>A	ENSP00000393597.2:p.Arg41=
ENST00000453956.1:c.121C>A	ENSP00000395442.1:p.Arg41=
NM_001136574.1:c.121C>A	NP_001130046.1:p.Arg41=
NM_001136575.1:c.121C>A	NP_001130047.1:p.Arg41=
NM_006055.2:c.121C>A	NP_006046.1:p.Arg41=
XM_005246243.2:c.157C>A	XP_005246300.1:p.Arg53=
NM_006055.3:c.121C>A MANE Select	NP_006046.1:p.Arg41=
NM_001136574.2:c.121C>A	NP_001130046.1:p.Arg41=
NM_001136575.2:c.121C>A	NP_001130047.1:p.Arg41=