Canonical Allele Identifier: CA362742835
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588855C>G , CM000668.2:g.6588855C>G GRCh38
NC_000006.11:g.6589088C>G , CM000668.1:g.6589088C>G GRCh37
NC_000006.10:g.6534087C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.121C>G (LY86) MANE Select ENSP00000230568.3:p.Leu41Val
ENST00000230568.4:c.121C>G (LY86) ENSP00000230568.3:p.Leu41Val
ENST00000379953.6:c.121C>G (LY86) ENSP00000369286.1:p.Leu41Val
NM_004271.3:c.121C>G (LY86) NP_004262.1:p.Leu41Val
NR_026970.1:n.196-19366G>C (LY86-AS1)
XM_017011505.1:c.121C>G (LY86) XP_016866994.1:p.Leu41Val
NM_004271.4:c.121C>G (LY86) MANE Select NP_004262.1:p.Leu41Val