Canonical Allele Identifier: CA565310682
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1263321801
gnomAD v2: 6-6610426-TACAC-T
gnomAD v3: 6-6610193-TACAC-T
gnomAD v4: 6-6610193-TACAC-T
MyVariant Identifiers: chr6:g.6610427_6610430del (hg19) chr6:g.6610194_6610197del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610194_6610197del , CM000668.2:g.6610194_6610197del GRCh38
NC_000006.11:g.6610427_6610430del , CM000668.1:g.6610427_6610430del GRCh37
NC_000006.10:g.6555426_6555429del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.137-14732_137-14729del (LY86) MANE Select ENSP00000230568.3:n.137-14732_137-14729del
ENST00000230568.4:c.137-14732_137-14729del (LY86) ENSP00000230568.3:n.137-14732_137-14729del
ENST00000379953.6:c.137-14732_137-14729del (LY86) ENSP00000369286.1:n.137-14732_137-14729del
NM_004271.3:c.137-14732_137-14729del (LY86) NP_004262.1:n.137-14732_137-14729del
NR_026970.1:n.195+12435_195+12438del (LY86-AS1)
XM_017011505.1:c.137-14732_137-14729del (LY86) XP_016866994.1:n.137-14732_137-14729del
NM_004271.4:c.137-14732_137-14729del (LY86) MANE Select NP_004262.1:n.137-14732_137-14729del
Search 100 bp 5'
Search 100 bp 3'