Canonical Allele Identifier: CA2677195818
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588959-G-GAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588959_6588960insAA , CM000668.2:g.6588959_6588960insAA GRCh38
NC_000006.11:g.6589192_6589193insAA , CM000668.1:g.6589192_6589193insAA GRCh37
NC_000006.10:g.6534191_6534192insAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+89_136+90insAA (LY86) MANE Select ENSP00000230568.3:n.136+89_136+90insAA
ENST00000230568.4:c.136+89_136+90insAA (LY86) ENSP00000230568.3:n.136+89_136+90insAA
ENST00000379953.6:c.136+89_136+90insAA (LY86) ENSP00000369286.1:n.136+89_136+90insAA
NM_004271.3:c.136+89_136+90insAA (LY86) NP_004262.1:n.136+89_136+90insAA
NR_026970.1:n.196-19471_196-19470insTT (LY86-AS1)
XM_017011505.1:c.136+89_136+90insAA (LY86) XP_016866994.1:n.136+89_136+90insAA
NM_004271.4:c.136+89_136+90insAA (LY86) MANE Select NP_004262.1:n.136+89_136+90insAA
Search 100 bp 5'
Search 100 bp 3'