Canonical Allele Identifier: CA2677195795
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588955_6588956dup , CM000668.2:g.6588955_6588956dup GRCh38
NC_000006.11:g.6589188_6589189dup , CM000668.1:g.6589188_6589189dup GRCh37
NC_000006.10:g.6534187_6534188dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+85_136+86dup (LY86) MANE Select ENSP00000230568.3:n.136+85_136+86dup
ENST00000230568.4:c.136+85_136+86dup (LY86) ENSP00000230568.3:n.136+85_136+86dup
ENST00000379953.6:c.136+85_136+86dup (LY86) ENSP00000369286.1:n.136+85_136+86dup
NM_004271.3:c.136+85_136+86dup (LY86) NP_004262.1:n.136+85_136+86dup
NR_026970.1:n.196-19465_196-19464dup (LY86-AS1)
XM_017011505.1:c.136+85_136+86dup (LY86) XP_016866994.1:n.136+85_136+86dup
NM_004271.4:c.136+85_136+86dup (LY86) MANE Select NP_004262.1:n.136+85_136+86dup