Canonical Allele Identifier: CA2677195788
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588952_6588959del , CM000668.2:g.6588952_6588959del GRCh38
NC_000006.11:g.6589185_6589192del , CM000668.1:g.6589185_6589192del GRCh37
NC_000006.10:g.6534184_6534191del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+82_136+89del (LY86) MANE Select ENSP00000230568.3:n.136+82_136+89del
ENST00000230568.4:c.136+82_136+89del (LY86) ENSP00000230568.3:n.136+82_136+89del
ENST00000379953.6:c.136+82_136+89del (LY86) ENSP00000369286.1:n.136+82_136+89del
NM_004271.3:c.136+82_136+89del (LY86) NP_004262.1:n.136+82_136+89del
NR_026970.1:n.196-19470_196-19463del (LY86-AS1)
XM_017011505.1:c.136+82_136+89del (LY86) XP_016866994.1:n.136+82_136+89del
NM_004271.4:c.136+82_136+89del (LY86) MANE Select NP_004262.1:n.136+82_136+89del