Canonical Allele Identifier: CA2578522443
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588890_6588892dup , CM000668.2:g.6588890_6588892dup GRCh38
NC_000006.11:g.6589123_6589125dup , CM000668.1:g.6589123_6589125dup GRCh37
NC_000006.10:g.6534122_6534124dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+20_136+22dup (LY86) MANE Select ENSP00000230568.3:n.136+20_136+22dup
ENST00000230568.4:c.136+20_136+22dup (LY86) ENSP00000230568.3:n.136+20_136+22dup
ENST00000379953.6:c.136+20_136+22dup (LY86) ENSP00000369286.1:n.136+20_136+22dup
NM_004271.3:c.136+20_136+22dup (LY86) NP_004262.1:n.136+20_136+22dup
NR_026970.1:n.196-19403_196-19401dup (LY86-AS1)
XM_017011505.1:c.136+20_136+22dup (LY86) XP_016866994.1:n.136+20_136+22dup
NM_004271.4:c.136+20_136+22dup (LY86) MANE Select NP_004262.1:n.136+20_136+22dup