Canonical Allele Identifier: CA2677195868
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588964-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588964_6588965insT , CM000668.2:g.6588964_6588965insT GRCh38
NC_000006.11:g.6589197_6589198insT , CM000668.1:g.6589197_6589198insT GRCh37
NC_000006.10:g.6534196_6534197insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+94_136+95insT (LY86) MANE Select ENSP00000230568.3:n.136+94_136+95insT
ENST00000230568.4:c.136+94_136+95insT (LY86) ENSP00000230568.3:n.136+94_136+95insT
ENST00000379953.6:c.136+94_136+95insT (LY86) ENSP00000369286.1:n.136+94_136+95insT
NM_004271.3:c.136+94_136+95insT (LY86) NP_004262.1:n.136+94_136+95insT
NR_026970.1:n.196-19476_196-19475insA (LY86-AS1)
XM_017011505.1:c.136+94_136+95insT (LY86) XP_016866994.1:n.136+94_136+95insT
NM_004271.4:c.136+94_136+95insT (LY86) MANE Select NP_004262.1:n.136+94_136+95insT