Canonical Allele Identifier: CA2769878353
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588958_6588959insA , CM000668.2:g.6588958_6588959insA GRCh38
NC_000006.11:g.6589191_6589192insA , CM000668.1:g.6589191_6589192insA GRCh37
NC_000006.10:g.6534190_6534191insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+88_136+89insA (LY86) MANE Select ENSP00000230568.3:n.136+88_136+89insA
ENST00000230568.4:c.136+88_136+89insA (LY86) ENSP00000230568.3:n.136+88_136+89insA
ENST00000379953.6:c.136+88_136+89insA (LY86) ENSP00000369286.1:n.136+88_136+89insA
NM_004271.3:c.136+88_136+89insA (LY86) NP_004262.1:n.136+88_136+89insA
NR_026970.1:n.196-19470_196-19469insT (LY86-AS1)
XM_017011505.1:c.136+88_136+89insA (LY86) XP_016866994.1:n.136+88_136+89insA
NM_004271.4:c.136+88_136+89insA (LY86) MANE Select NP_004262.1:n.136+88_136+89insA