Canonical Allele Identifier: CA917667622
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1561771540
gnomAD v4: 6-6588961-A-AGG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588964_6588965dup , CM000668.2:g.6588964_6588965dup GRCh38
NC_000006.11:g.6589197_6589198dup , CM000668.1:g.6589197_6589198dup GRCh37
NC_000006.10:g.6534196_6534197dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+94_136+95dup (LY86) MANE Select ENSP00000230568.3:n.136+94_136+95dup
ENST00000230568.4:c.136+94_136+95dup (LY86) ENSP00000230568.3:n.136+94_136+95dup
ENST00000379953.6:c.136+94_136+95dup (LY86) ENSP00000369286.1:n.136+94_136+95dup
NM_004271.3:c.136+94_136+95dup (LY86) NP_004262.1:n.136+94_136+95dup
NR_026970.1:n.196-19474_196-19473dup (LY86-AS1)
XM_017011505.1:c.136+94_136+95dup (LY86) XP_016866994.1:n.136+94_136+95dup
NM_004271.4:c.136+94_136+95dup (LY86) MANE Select NP_004262.1:n.136+94_136+95dup
Search 100 bp 5'
Search 100 bp 3'