Canonical Allele Identifier: CA1608139858
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588962_6588978delinsGGGGAGAGGGGACCAGC , CM000668.2:g.6588962_6588978delinsGGGGAGAGGGGACCAGC GRCh38
NC_000006.11:g.6589195_6589211delinsGGGGAGAGGGGACCAGC , CM000668.1:g.6589195_6589211delinsGGGGAGAGGGGACCAGC GRCh37
NC_000006.10:g.6534194_6534210delinsGGGGAGAGGGGACCAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) MANE Select ENSP00000230568.3:n.136+92_136+108delinsGGGGAGAGGGGACCAGC
ENST00000230568.4:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) ENSP00000230568.3:n.136+92_136+108delinsGGGGAGAGGGGACCAGC
ENST00000379953.6:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) ENSP00000369286.1:n.136+92_136+108delinsGGGGAGAGGGGACCAGC
NM_004271.3:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) NP_004262.1:n.136+92_136+108delinsGGGGAGAGGGGACCAGC
NR_026970.1:n.196-19489_196-19473delinsGCTGGTCCCCTCTCCCC (LY86-AS1)
XM_017011505.1:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) XP_016866994.1:n.136+92_136+108delinsGGGGAGAGGGGACCAGC
NM_004271.4:c.136+92_136+108delinsGGGGAGAGGGGACCAGC (LY86) MANE Select NP_004262.1:n.136+92_136+108delinsGGGGAGAGGGGACCAGC