Canonical Allele Identifier: CA565308665
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1308068667
gnomAD v2: 6-6589190-TGGGAG-T
gnomAD v3: 6-6588957-TGGGAG-T
gnomAD v4: 6-6588957-TGGGAG-T
MyVariant Identifiers: chr6:g.6589191_6589195del (hg19) chr6:g.6588958_6588962del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588963_6588967del , CM000668.2:g.6588963_6588967del GRCh38
NC_000006.11:g.6589196_6589200del , CM000668.1:g.6589196_6589200del GRCh37
NC_000006.10:g.6534195_6534199del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+93_136+97del (LY86) MANE Select ENSP00000230568.3:n.136+93_136+97del
ENST00000230568.4:c.136+93_136+97del (LY86) ENSP00000230568.3:n.136+93_136+97del
ENST00000379953.6:c.136+93_136+97del (LY86) ENSP00000369286.1:n.136+93_136+97del
NM_004271.3:c.136+93_136+97del (LY86) NP_004262.1:n.136+93_136+97del
NR_026970.1:n.196-19473_196-19469del (LY86-AS1)
XM_017011505.1:c.136+93_136+97del (LY86) XP_016866994.1:n.136+93_136+97del
NM_004271.4:c.136+93_136+97del (LY86) MANE Select NP_004262.1:n.136+93_136+97del
Search 100 bp 5'
Search 100 bp 3'