Canonical Allele Identifier: CA1085659265
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1761296004
gnomAD v3: 6-6610180-A-ACAGT
gnomAD v4: 6-6610180-A-ACAGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610182_6610185dup , CM000668.2:g.6610182_6610185dup GRCh38
NC_000006.11:g.6610415_6610418dup , CM000668.1:g.6610415_6610418dup GRCh37
NC_000006.10:g.6555414_6555417dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.137-14744_137-14741dup (LY86) MANE Select ENSP00000230568.3:n.137-14744_137-14741dup
ENST00000230568.4:c.137-14744_137-14741dup (LY86) ENSP00000230568.3:n.137-14744_137-14741dup
ENST00000379953.6:c.137-14744_137-14741dup (LY86) ENSP00000369286.1:n.137-14744_137-14741dup
NM_004271.3:c.137-14744_137-14741dup (LY86) NP_004262.1:n.137-14744_137-14741dup
NR_026970.1:n.195+12448_195+12451dup (LY86-AS1)
XM_017011505.1:c.137-14744_137-14741dup (LY86) XP_016866994.1:n.137-14744_137-14741dup
NM_004271.4:c.137-14744_137-14741dup (LY86) MANE Select NP_004262.1:n.137-14744_137-14741dup
Search 100 bp 5'
Search 100 bp 3'