Canonical Allele Identifier: CA134433547
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs145808577
MyVariant Identifiers: chr6:g.6588980_6588981insCCCC (hg19) chr6:g.6588747_6588748insCCCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588748_6588749insCCCC , CM000668.2:g.6588748_6588749insCCCC GRCh38
NC_000006.11:g.6588981_6588982insCCCC , CM000668.1:g.6588981_6588982insCCCC GRCh37
NC_000006.10:g.6533980_6533981insCCCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.14_15insCCCC (LY86) MANE Select ENSP00000230568.3:p.Ala6ProfsTer30
ENST00000230568.4:c.14_15insCCCC (LY86) ENSP00000230568.3:p.Ala6ProfsTer30
ENST00000379953.6:c.14_15insCCCC (LY86) ENSP00000369286.1:p.Ala6ProfsTer30
NM_004271.3:c.14_15insCCCC (LY86) NP_004262.1:p.Ala6ProfsTer30
NR_026970.1:n.196-19259_196-19258insGGGG (LY86-AS1)
XM_017011505.1:c.14_15insCCCC (LY86) XP_016866994.1:p.Ala6ProfsTer30
NM_004271.4:c.14_15insCCCC (LY86) MANE Select NP_004262.1:p.Ala6ProfsTer30
Search 100 bp 5'
Search 100 bp 3'