Canonical Allele Identifier: CA1085646999
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760427851

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588729_6588731dup , CM000668.2:g.6588729_6588731dup GRCh38
NC_000006.11:g.6588962_6588964dup , CM000668.1:g.6588962_6588964dup GRCh37
NC_000006.10:g.6533961_6533963dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.-6_-4dup (LY86) MANE Select ENSP00000230568.3:n.-6_-4dup
ENST00000230568.4:c.-6_-4dup (LY86) ENSP00000230568.3:n.-6_-4dup
ENST00000379953.6:c.-6_-4dup (LY86) ENSP00000369286.1:n.-6_-4dup
NM_004271.3:c.-6_-4dup (LY86) NP_004262.1:n.-6_-4dup
NR_026970.1:n.196-19240_196-19238dup (LY86-AS1)
XM_017011505.1:c.-6_-4dup (LY86) XP_016866994.1:n.-6_-4dup
NM_004271.4:c.-6_-4dup (LY86) MANE Select NP_004262.1:n.-6_-4dup