Canonical Allele Identifier: CA2493923916
Community Standard Title: NM_016008.4(DYNC2LI1):c.993+3A=
Gene: DYNC2LI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43805249A= , CM000664.2:g.43805249A= GRCh38
NC_000002.11:g.44032388A= , CM000664.1:g.44032388A= GRCh37
NC_000002.10:g.43885892A= NCBI36
NG_053008.1:g.36211A=

Transcript Alleles

HGVS Amino-acid Change
NM_016008.4:c.993+3A= MANE Select NP_057092.2:n.993+3A=
ENST00000260605.12:c.993+3A= MANE Select ENSP00000260605.8:n.993+3A=
NM_001193464.1:c.996+3A= NP_001180393.1:n.996+3A=
NM_001193464.2:c.996+3A= NP_001180393.1:n.996+3A=
NM_001348912.1:c.993+3A= NP_001335841.1:n.993+3A=
NM_001348912.2:c.993+3A= NP_001335841.1:n.993+3A=
NM_001348913.1:c.996+3A= NP_001335842.1:n.996+3A=
NM_001348913.2:c.996+3A= NP_001335842.1:n.996+3A=
NM_016008.3:c.993+3A= NP_057092.2:n.993+3A=
ENST00000378587.3:c.947A=
ENST00000605786.5:c.996+3A= ENSP00000474032.1:n.996+3A=
XM_005264364.3:c.996+3A= XP_005264421.1:n.996+3A=
XM_005264365.3:c.993+3A= XP_005264422.1:n.993+3A=