Canonical Allele Identifier: CA2677195809
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588958-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588958_6588959insT , CM000668.2:g.6588958_6588959insT GRCh38
NC_000006.11:g.6589191_6589192insT , CM000668.1:g.6589191_6589192insT GRCh37
NC_000006.10:g.6534190_6534191insT NCBI36

Transcript Alleles

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