Canonical Allele Identifier: CA1635956
Community Standard Title: NM_016008.4(DYNC2LI1):c.655-9del
Gene: DYNC2LI1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43800832del , CM000664.2:g.43800832del GRCh38
NC_000002.11:g.44027971del , CM000664.1:g.44027971del GRCh37
NC_000002.10:g.43881475del NCBI36
NG_053008.1:g.31794del

Transcript Alleles

HGVS Amino-acid Change
NM_016008.4:c.655-9del MANE Select NP_057092.2:n.655-9del
ENST00000260605.12:c.655-9del MANE Select ENSP00000260605.8:n.655-9del
NM_001193464.1:c.658-9del NP_001180393.1:n.658-9del
NM_001193464.2:c.658-9del NP_001180393.1:n.658-9del
NM_001348912.1:c.655-9del NP_001335841.1:n.655-9del
NM_001348912.2:c.655-9del NP_001335841.1:n.655-9del
NM_001348913.1:c.658-9del NP_001335842.1:n.658-9del
NM_001348913.2:c.658-9del NP_001335842.1:n.658-9del
NM_016008.3:c.655-9del NP_057092.2:n.655-9del
ENST00000378587.3:c.606-9del
ENST00000489222.6:n.611-9del
ENST00000605786.5:c.658-9del ENSP00000474032.1:n.658-9del
XM_005264364.3:c.658-9del XP_005264421.1:n.658-9del
XM_005264365.3:c.655-9del XP_005264422.1:n.655-9del
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