Canonical Allele Identifier: CA2677195877
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588965-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588965_6588966insT , CM000668.2:g.6588965_6588966insT GRCh38
NC_000006.11:g.6589198_6589199insT , CM000668.1:g.6589198_6589199insT GRCh37
NC_000006.10:g.6534197_6534198insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+95_136+96insT (LY86) MANE Select ENSP00000230568.3:n.136+95_136+96insT
ENST00000230568.4:c.136+95_136+96insT (LY86) ENSP00000230568.3:n.136+95_136+96insT
ENST00000379953.6:c.136+95_136+96insT (LY86) ENSP00000369286.1:n.136+95_136+96insT
NM_004271.3:c.136+95_136+96insT (LY86) NP_004262.1:n.136+95_136+96insT
NR_026970.1:n.196-19477_196-19476insA (LY86-AS1)
XM_017011505.1:c.136+95_136+96insT (LY86) XP_016866994.1:n.136+95_136+96insT
NM_004271.4:c.136+95_136+96insT (LY86) MANE Select NP_004262.1:n.136+95_136+96insT