Canonical Allele Identifier: CA448646251

Gene: LY86 LY86-AS1

Linked Data

• MyVariant Identifiers: chr6:g.6589009T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6588776T>C , CM000668.2:g.6588776T>C	GRCh38
NC_000006.11:g.6589009T>C , CM000668.1:g.6589009T>C	GRCh37
NC_000006.10:g.6534008T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230568.5:c.42T>C (LY86) MANE Select	ENSP00000230568.3:p.Ile14=
ENST00000230568.4:c.42T>C (LY86)	ENSP00000230568.3:p.Ile14=
ENST00000379953.6:c.42T>C (LY86)	ENSP00000369286.1:p.Ile14=
NM_004271.3:c.42T>C (LY86)	NP_004262.1:p.Ile14=
NR_026970.1:n.196-19287A>G (LY86-AS1)
XM_017011505.1:c.42T>C (LY86)	XP_016866994.1:p.Ile14=
NM_004271.4:c.42T>C (LY86) MANE Select	NP_004262.1:p.Ile14=