Canonical Allele Identifier: CA1608170506
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610268C= , CM000668.2:g.6610268C= GRCh38
NC_000006.11:g.6610501C= , CM000668.1:g.6610501C= GRCh37
NC_000006.10:g.6555500C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230568.5:c.137-14658C= (LY86) MANE Select ENSP00000230568.3:n.137-14658C=
ENST00000230568.4:c.137-14658C= (LY86) ENSP00000230568.3:n.137-14658C=
ENST00000379953.6:c.137-14658C= (LY86) ENSP00000369286.1:n.137-14658C=
NM_004271.3:c.137-14658C= (LY86) NP_004262.1:n.137-14658C=
NR_026970.1:n.195+12364G= (LY86-AS1)
XM_017011505.1:c.137-14658C= (LY86) XP_016866994.1:n.137-14658C=
NM_004271.4:c.137-14658C= (LY86) MANE Select NP_004262.1:n.137-14658C=
Search 100 bp 5'
Search 100 bp 3'