Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA827150081

Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1389366997

gnomAD v3: 6-6588661-A-AG

gnomAD v4: 6-6588661-A-AG

MyVariant Identifiers: chr6:g.6588894_6588895insG (hg19) chr6:g.6588661_6588662insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6588665dup , CM000668.2:g.6588665dup	GRCh38
NC_000006.11:g.6588898dup , CM000668.1:g.6588898dup	GRCh37
NC_000006.10:g.6533897dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379953.6:c.-9-61dup (LY86)	ENSP00000369286.1:n.-9-61dup
NR_026970.1:n.196-19173dup (LY86-AS1)
XM_017011505.1:c.-70dup (LY86)	XP_016866994.1:n.-70dup

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