Canonical Allele Identifier: CA1608170525
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610299_6610300delinsTC , CM000668.2:g.6610299_6610300delinsTC GRCh38
NC_000006.11:g.6610532_6610533delinsTC , CM000668.1:g.6610532_6610533delinsTC GRCh37
NC_000006.10:g.6555531_6555532delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230568.5:c.137-14627_137-14626delinsTC (LY86) MANE Select ENSP00000230568.3:n.137-14627_137-14626de...
ENST00000230568.4:c.137-14627_137-14626delinsTC (LY86) ENSP00000230568.3:n.137-14627_137-14626de...
ENST00000379953.6:c.137-14627_137-14626delinsTC (LY86) ENSP00000369286.1:n.137-14627_137-14626de...
NM_004271.3:c.137-14627_137-14626delinsTC (LY86) NP_004262.1:n.137-14627_137-14626delinsTC...
NR_026970.1:n.195+12332_195+12333delinsGA (LY86-AS1)
XM_017011505.1:c.137-14627_137-14626delinsTC (LY86) XP_016866994.1:n.137-14627_137-14626delin...
NM_004271.4:c.137-14627_137-14626delinsTC (LY86) MANE Select NP_004262.1:n.137-14627_137-14626delinsTC...