Canonical Allele Identifier: CA1608170518
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610287_6610289delinsCTT , CM000668.2:g.6610287_6610289delinsCTT GRCh38
NC_000006.11:g.6610520_6610522delinsCTT , CM000668.1:g.6610520_6610522delinsCTT GRCh37
NC_000006.10:g.6555519_6555521delinsCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230568.5:c.137-14639_137-14637delinsCTT (LY86) MANE Select ENSP00000230568.3:n.137-14639_137-14637de...
ENST00000230568.4:c.137-14639_137-14637delinsCTT (LY86) ENSP00000230568.3:n.137-14639_137-14637de...
ENST00000379953.6:c.137-14639_137-14637delinsCTT (LY86) ENSP00000369286.1:n.137-14639_137-14637de...
NM_004271.3:c.137-14639_137-14637delinsCTT (LY86) NP_004262.1:n.137-14639_137-14637delinsCT...
NR_026970.1:n.195+12343_195+12345delinsAAG (LY86-AS1)
XM_017011505.1:c.137-14639_137-14637delinsCTT (LY86) XP_016866994.1:n.137-14639_137-14637delin...
NM_004271.4:c.137-14639_137-14637delinsCTT (LY86) MANE Select NP_004262.1:n.137-14639_137-14637delinsCT...