Canonical Allele Identifier: CA134433563
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs35589645
gnomAD v2: 6-6589193-G-GAA
gnomAD v3: 6-6588960-G-GAA
gnomAD v4: 6-6588960-G-GAA
MyVariant Identifiers: chr6:g.6589193_6589194insAA (hg19) chr6:g.6588960_6588961insAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588961_6588962insAA , CM000668.2:g.6588961_6588962insAA GRCh38
NC_000006.11:g.6589194_6589195insAA , CM000668.1:g.6589194_6589195insAA GRCh37
NC_000006.10:g.6534193_6534194insAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+91_136+92insAA (LY86) MANE Select ENSP00000230568.3:n.136+91_136+92insAA
ENST00000230568.4:c.136+91_136+92insAA (LY86) ENSP00000230568.3:n.136+91_136+92insAA
ENST00000379953.6:c.136+91_136+92insAA (LY86) ENSP00000369286.1:n.136+91_136+92insAA
NM_004271.3:c.136+91_136+92insAA (LY86) NP_004262.1:n.136+91_136+92insAA
NR_026970.1:n.196-19472_196-19471insTT (LY86-AS1)
XM_017011505.1:c.136+91_136+92insAA (LY86) XP_016866994.1:n.136+91_136+92insAA
NM_004271.4:c.136+91_136+92insAA (LY86) MANE Select NP_004262.1:n.136+91_136+92insAA
Search 100 bp 5'
Search 100 bp 3'