Canonical Allele Identifier: CA2677195941
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-6588993-TC-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588995del , CM000668.2:g.6588995del GRCh38
NC_000006.11:g.6589228del , CM000668.1:g.6589228del GRCh37
NC_000006.10:g.6534227del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.136+125del (LY86) MANE Select ENSP00000230568.3:n.136+125del
ENST00000230568.4:c.136+125del (LY86) ENSP00000230568.3:n.136+125del
ENST00000379953.6:c.136+125del (LY86) ENSP00000369286.1:n.136+125del
NM_004271.3:c.136+125del (LY86) NP_004262.1:n.136+125del
NR_026970.1:n.196-19505del (LY86-AS1)
XM_017011505.1:c.136+125del (LY86) XP_016866994.1:n.136+125del
NM_004271.4:c.136+125del (LY86) MANE Select NP_004262.1:n.136+125del