Canonical Allele Identifier: CA1608170543
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610336_6610338delinsATT , CM000668.2:g.6610336_6610338delinsATT GRCh38
NC_000006.11:g.6610569_6610571delinsATT , CM000668.1:g.6610569_6610571delinsATT GRCh37
NC_000006.10:g.6555568_6555570delinsATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.137-14590_137-14588delinsATT (LY86) MANE Select ENSP00000230568.3:n.137-14590_137-14588delinsATT
ENST00000230568.4:c.137-14590_137-14588delinsATT (LY86) ENSP00000230568.3:n.137-14590_137-14588delinsATT
ENST00000379953.6:c.137-14590_137-14588delinsATT (LY86) ENSP00000369286.1:n.137-14590_137-14588delinsATT
NM_004271.3:c.137-14590_137-14588delinsATT (LY86) NP_004262.1:n.137-14590_137-14588delinsATT
NR_026970.1:n.195+12294_195+12296delinsAAT (LY86-AS1)
XM_017011505.1:c.137-14590_137-14588delinsATT (LY86) XP_016866994.1:n.137-14590_137-14588delinsATT
NM_004271.4:c.137-14590_137-14588delinsATT (LY86) MANE Select NP_004262.1:n.137-14590_137-14588delinsATT
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