Canonical Allele Identifier: CA2677195713
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2113062459

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588732_6588733dup , CM000668.2:g.6588732_6588733dup GRCh38
NC_000006.11:g.6588965_6588966dup , CM000668.1:g.6588965_6588966dup GRCh37
NC_000006.10:g.6533964_6533965dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.-3_-2dup (LY86) MANE Select ENSP00000230568.3:n.-3_-2dup
ENST00000230568.4:c.-3_-2dup (LY86) ENSP00000230568.3:n.-3_-2dup
ENST00000379953.6:c.-3_-2dup (LY86) ENSP00000369286.1:n.-3_-2dup
NM_004271.3:c.-3_-2dup (LY86) NP_004262.1:n.-3_-2dup
NR_026970.1:n.196-19243_196-19242dup (LY86-AS1)
XM_017011505.1:c.-3_-2dup (LY86) XP_016866994.1:n.-3_-2dup
NM_004271.4:c.-3_-2dup (LY86) MANE Select NP_004262.1:n.-3_-2dup