Canonical Allele Identifier: CA2677195862
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588963-G-GA

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588963_6588964insA , CM000668.2:g.6588963_6588964insA GRCh38
NC_000006.11:g.6589196_6589197insA , CM000668.1:g.6589196_6589197insA GRCh37
NC_000006.10:g.6534195_6534196insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+93_136+94insA (LY86) MANE Select ENSP00000230568.3:n.136+93_136+94insA
ENST00000230568.4:c.136+93_136+94insA (LY86) ENSP00000230568.3:n.136+93_136+94insA
ENST00000379953.6:c.136+93_136+94insA (LY86) ENSP00000369286.1:n.136+93_136+94insA
NM_004271.3:c.136+93_136+94insA (LY86) NP_004262.1:n.136+93_136+94insA
NR_026970.1:n.196-19475_196-19474insT (LY86-AS1)
XM_017011505.1:c.136+93_136+94insA (LY86) XP_016866994.1:n.136+93_136+94insA
NM_004271.4:c.136+93_136+94insA (LY86) MANE Select NP_004262.1:n.136+93_136+94insA