Canonical Allele Identifier: CA134433564
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs386406026
MyVariant Identifiers: chr6:g.6589194_6589195insAG (hg19) chr6:g.6588961_6588962insAG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588961_6588962insAG , CM000668.2:g.6588961_6588962insAG GRCh38
NC_000006.11:g.6589194_6589195insAG , CM000668.1:g.6589194_6589195insAG GRCh37
NC_000006.10:g.6534193_6534194insAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+91_136+92insAG (LY86) MANE Select ENSP00000230568.3:n.136+91_136+92insAG
ENST00000230568.4:c.136+91_136+92insAG (LY86) ENSP00000230568.3:n.136+91_136+92insAG
ENST00000379953.6:c.136+91_136+92insAG (LY86) ENSP00000369286.1:n.136+91_136+92insAG
NM_004271.3:c.136+91_136+92insAG (LY86) NP_004262.1:n.136+91_136+92insAG
NR_026970.1:n.196-19473_196-19472insCT (LY86-AS1)
XM_017011505.1:c.136+91_136+92insAG (LY86) XP_016866994.1:n.136+91_136+92insAG
NM_004271.4:c.136+91_136+92insAG (LY86) MANE Select NP_004262.1:n.136+91_136+92insAG
Search 100 bp 5'
Search 100 bp 3'