Canonical Allele Identifier: CA1608139687
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588831_6588832delinsTG , CM000668.2:g.6588831_6588832delinsTG GRCh38
NC_000006.11:g.6589064_6589065delinsTG , CM000668.1:g.6589064_6589065delinsTG GRCh37
NC_000006.10:g.6534063_6534064delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.97_98delinsTG (LY86) MANE Select ENSP00000230568.3:p.Cys33=
ENST00000230568.4:c.97_98delinsTG (LY86) ENSP00000230568.3:p.Cys33=
ENST00000379953.6:c.97_98delinsTG (LY86) ENSP00000369286.1:p.Cys33=
NM_004271.3:c.97_98delinsTG (LY86) NP_004262.1:p.Cys33=
NR_026970.1:n.196-19343_196-19342delinsCA (LY86-AS1)
XM_017011505.1:c.97_98delinsTG (LY86) XP_016866994.1:p.Cys33=
NM_004271.4:c.97_98delinsTG (LY86) MANE Select NP_004262.1:p.Cys33=