Canonical Allele Identifier: CA1085647012
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760430258
gnomAD v3: 6-6588753-ACT-A
gnomAD v4: 6-6588753-ACT-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588758_6588759del , CM000668.2:g.6588758_6588759del GRCh38
NC_000006.11:g.6588991_6588992del , CM000668.1:g.6588991_6588992del GRCh37
NC_000006.10:g.6533990_6533991del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.24_25del (LY86) MANE Select ENSP00000230568.3:p.Phe9ProfsTer25
ENST00000230568.4:c.24_25del (LY86) ENSP00000230568.3:p.Phe9ProfsTer25
ENST00000379953.6:c.24_25del (LY86) ENSP00000369286.1:p.Phe9ProfsTer25
NM_004271.3:c.24_25del (LY86) NP_004262.1:p.Phe9ProfsTer25
NR_026970.1:n.196-19266_196-19265del (LY86-AS1)
XM_017011505.1:c.24_25del (LY86) XP_016866994.1:p.Phe9ProfsTer25
NM_004271.4:c.24_25del (LY86) MANE Select NP_004262.1:p.Phe9ProfsTer25
Search 100 bp 5'
Search 100 bp 3'