Canonical Allele Identifier: CA827150593
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1554122325
MyVariant Identifiers: chr6:g.6589192_6589193insGGA (hg19) chr6:g.6588959_6588960insGGA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588960_6588961insGAG , CM000668.2:g.6588960_6588961insGAG GRCh38
NC_000006.11:g.6589193_6589194insGAG , CM000668.1:g.6589193_6589194insGAG GRCh37
NC_000006.10:g.6534192_6534193insGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+90_136+91insGAG (LY86) MANE Select ENSP00000230568.3:n.136+90_136+91insGAG
ENST00000230568.4:c.136+90_136+91insGAG (LY86) ENSP00000230568.3:n.136+90_136+91insGAG
ENST00000379953.6:c.136+90_136+91insGAG (LY86) ENSP00000369286.1:n.136+90_136+91insGAG
NM_004271.3:c.136+90_136+91insGAG (LY86) NP_004262.1:n.136+90_136+91insGAG
NR_026970.1:n.196-19471_196-19470insTCC (LY86-AS1)
XM_017011505.1:c.136+90_136+91insGAG (LY86) XP_016866994.1:n.136+90_136+91insGAG
NM_004271.4:c.136+90_136+91insGAG (LY86) MANE Select NP_004262.1:n.136+90_136+91insGAG
Search 100 bp 5'
Search 100 bp 3'