Canonical Allele Identifier: CA2677195753

Gene: LY86 LY86-AS1

Linked Data

• gnomAD v4: 6-6588931-C-CACTAGCGGCTCACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6588931_6588932insACTAGCGGCTCACAT , CM000668.2:g.6588931_6588932insACTAGCGGCTCACAT	GRCh38
NC_000006.11:g.6589164_6589165insACTAGCGGCTCACAT , CM000668.1:g.6589164_6589165insACTAGCGGCTCACAT	GRCh37
NC_000006.10:g.6534163_6534164insACTAGCGGCTCACAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230568.5:c.136+61_136+62insACTAGCGGCTCACAT (LY86) MANE Select	ENSP00000230568.3:n.136+61_136+62insACTAGCGGCTCACAT
ENST00000230568.4:c.136+61_136+62insACTAGCGGCTCACAT (LY86)	ENSP00000230568.3:n.136+61_136+62insACTAGCGGCTCACAT
ENST00000379953.6:c.136+61_136+62insACTAGCGGCTCACAT (LY86)	ENSP00000369286.1:n.136+61_136+62insACTAGCGGCTCACAT
NM_004271.3:c.136+61_136+62insACTAGCGGCTCACAT (LY86)	NP_004262.1:n.136+61_136+62insACTAGCGGCTCACAT
NR_026970.1:n.196-19443_196-19442insATGTGAGCCGCTAGT (LY86-AS1)
XM_017011505.1:c.136+61_136+62insACTAGCGGCTCACAT (LY86)	XP_016866994.1:n.136+61_136+62insACTAGCGGCTCACAT
NM_004271.4:c.136+61_136+62insACTAGCGGCTCACAT (LY86) MANE Select	NP_004262.1:n.136+61_136+62insACTAGCGGCTCACAT