Canonical Allele Identifier: CA2830536290

Gene: LMLN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.198002780del , CM000665.2:g.198002780del	GRCh38
NC_000003.11:g.197729651del , CM000665.1:g.197729651del	GRCh37
NC_000003.10:g.199214048del	NCBI36
NG_047207.1:g.47581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420910.7:c.1209-235del MANE Select	ENSP00000410926.3:n.1209-235del
ENST00000330198.8:c.1232+3438del	ENSP00000328829.4:n.1232+3438del
ENST00000332636.5:c.1076+3438del	ENSP00000328611.5:n.1076+3438del
ENST00000420910.6:c.1233-235del	ENSP00000410926.2:n.1233-235del
ENST00000451139.6:n.1724-235del
ENST00000476356.5:n.434+3438del
ENST00000482695.5:c.1077-235del	ENSP00000418324.1:n.1077-235del
NM_001136049.2:c.1233-235del	NP_001129521.2:n.1233-235del
NM_033029.3:c.1232+3438del	NP_149018.2:n.1232+3438del
NR_026786.1:n.1134-235del
NR_026787.1:n.1133+3438del
XM_011513270.1:c.1218-235del	XP_011511572.1:n.1218-235del
XM_011513271.1:c.1233-235del	XP_011511573.1:n.1233-235del
XM_011513272.1:c.1233-235del	XP_011511574.1:n.1233-235del
NR_026786.2:n.1117-235del
NR_026787.2:n.1116+3438del
NM_001136049.3:c.1209-235del MANE Select	NP_001129521.3:n.1209-235del
NM_033029.4:c.1208+3438del	NP_149018.3:n.1208+3438del