Canonical Allele Identifier: CA2769878351
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588933_6588934insT , CM000668.2:g.6588933_6588934insT GRCh38
NC_000006.11:g.6589166_6589167insT , CM000668.1:g.6589166_6589167insT GRCh37
NC_000006.10:g.6534165_6534166insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+63_136+64insT (LY86) MANE Select ENSP00000230568.3:n.136+63_136+64insT
ENST00000230568.4:c.136+63_136+64insT (LY86) ENSP00000230568.3:n.136+63_136+64insT
ENST00000379953.6:c.136+63_136+64insT (LY86) ENSP00000369286.1:n.136+63_136+64insT
NM_004271.3:c.136+63_136+64insT (LY86) NP_004262.1:n.136+63_136+64insT
NR_026970.1:n.196-19445_196-19444insA (LY86-AS1)
XM_017011505.1:c.136+63_136+64insT (LY86) XP_016866994.1:n.136+63_136+64insT
NM_004271.4:c.136+63_136+64insT (LY86) MANE Select NP_004262.1:n.136+63_136+64insT