Canonical Allele Identifier: CA2578522457
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2113063257
gnomAD v4: 6-6588961-A-AGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588962_6588963insTG , CM000668.2:g.6588962_6588963insTG GRCh38
NC_000006.11:g.6589195_6589196insTG , CM000668.1:g.6589195_6589196insTG GRCh37
NC_000006.10:g.6534194_6534195insTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+92_136+93insTG (LY86) MANE Select ENSP00000230568.3:n.136+92_136+93insTG
ENST00000230568.4:c.136+92_136+93insTG (LY86) ENSP00000230568.3:n.136+92_136+93insTG
ENST00000379953.6:c.136+92_136+93insTG (LY86) ENSP00000369286.1:n.136+92_136+93insTG
NM_004271.3:c.136+92_136+93insTG (LY86) NP_004262.1:n.136+92_136+93insTG
NR_026970.1:n.196-19473_196-19472insAC (LY86-AS1)
XM_017011505.1:c.136+92_136+93insTG (LY86) XP_016866994.1:n.136+92_136+93insTG
NM_004271.4:c.136+92_136+93insTG (LY86) MANE Select NP_004262.1:n.136+92_136+93insTG
Search 100 bp 5'
Search 100 bp 3'