Canonical Allele Identifier: CA362742659
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588789A>C , CM000668.2:g.6588789A>C GRCh38
NC_000006.11:g.6589022A>C , CM000668.1:g.6589022A>C GRCh37
NC_000006.10:g.6534021A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.55A>C (LY86) MANE Select ENSP00000230568.3:p.Ser19Arg
ENST00000230568.4:c.55A>C (LY86) ENSP00000230568.3:p.Ser19Arg
ENST00000379953.6:c.55A>C (LY86) ENSP00000369286.1:p.Ser19Arg
NM_004271.3:c.55A>C (LY86) NP_004262.1:p.Ser19Arg
NR_026970.1:n.196-19300T>G (LY86-AS1)
XM_017011505.1:c.55A>C (LY86) XP_016866994.1:p.Ser19Arg
NM_004271.4:c.55A>C (LY86) MANE Select NP_004262.1:p.Ser19Arg