Canonical Allele Identifier: CA2677195716
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588828-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588829dup , CM000668.2:g.6588829dup GRCh38
NC_000006.11:g.6589062dup , CM000668.1:g.6589062dup GRCh37
NC_000006.10:g.6534061dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.95dup (LY86) MANE Select ENSP00000230568.3:p.Cys33LeufsTer2
ENST00000230568.4:c.95dup (LY86) ENSP00000230568.3:p.Cys33LeufsTer2
ENST00000379953.6:c.95dup (LY86) ENSP00000369286.1:p.Cys33LeufsTer2
NM_004271.3:c.95dup (LY86) NP_004262.1:p.Cys33LeufsTer2
NR_026970.1:n.196-19340dup (LY86-AS1)
XM_017011505.1:c.95dup (LY86) XP_016866994.1:p.Cys33LeufsTer2
NM_004271.4:c.95dup (LY86) MANE Select NP_004262.1:p.Cys33LeufsTer2