Canonical Allele Identifier: CA2493923915
Community Standard Title: NM_016008.4(DYNC2LI1):c.993+1G=
Gene: DYNC2LI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43805247G= , CM000664.2:g.43805247G= GRCh38
NC_000002.11:g.44032386G= , CM000664.1:g.44032386G= GRCh37
NC_000002.10:g.43885890G= NCBI36
NG_053008.1:g.36209G=

Transcript Alleles

HGVS Amino-acid Change
NM_016008.4:c.993+1G= MANE Select NP_057092.2:n.993+1G=
ENST00000260605.12:c.993+1G= MANE Select ENSP00000260605.8:n.993+1G=
NM_001193464.1:c.996+1G= NP_001180393.1:n.996+1G=
NM_001193464.2:c.996+1G= NP_001180393.1:n.996+1G=
NM_001348912.1:c.993+1G= NP_001335841.1:n.993+1G=
NM_001348912.2:c.993+1G= NP_001335841.1:n.993+1G=
NM_001348913.1:c.996+1G= NP_001335842.1:n.996+1G=
NM_001348913.2:c.996+1G= NP_001335842.1:n.996+1G=
NM_016008.3:c.993+1G= NP_057092.2:n.993+1G=
ENST00000378587.3:c.945G=
ENST00000605786.5:c.996+1G= ENSP00000474032.1:n.996+1G=
XM_005264364.3:c.996+1G= XP_005264421.1:n.996+1G=
XM_005264365.3:c.993+1G= XP_005264422.1:n.993+1G=