Canonical Allele Identifier: CA1764914323
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13086182C= , CM000670.2:g.13086182C= GRCh38
NC_000008.10:g.12943691C= , CM000670.1:g.12943691C= GRCh37
NC_000008.9:g.12988062C= NCBI36
NG_015998.1:g.433739G=
NG_015998.2:g.523424G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276297.9:c.4466+108G= MANE Select ENSP00000276297.4:n.4466+108G=
ENST00000276297.8:c.4466+108G= ENSP00000276297.4:n.4466+108G=
ENST00000358919.6:c.3155+108G= ENSP00000351797.2:n.3155+108G=
ENST00000510318.5:n.1651+108G=
ENST00000512044.6:c.3257+108G= ENSP00000422595.2:n.3257+108G=
ENST00000520226.5:c.2933+108G= ENSP00000428028.1:n.2933+108G=
NM_001164271.1:c.2933+108G= NP_001157743.1:n.2933+108G=
NM_001316668.1:c.3257+108G= NP_001303597.1:n.3257+108G=
NM_006094.4:c.3155+108G= NP_006085.2:n.3155+108G=
NM_182643.2:c.4466+108G= NP_872584.2:n.4466+108G=
XM_005273374.1:c.4466+108G= XP_005273431.1:n.4466+108G=
NM_001348081.1:c.4466+108G= NP_001335010.1:n.4466+108G=
NM_001348082.1:c.2933+108G= NP_001335011.1:n.2933+108G=
NM_001348083.1:c.2933+108G= NP_001335012.1:n.2933+108G=
NM_001348084.1:c.2933+108G= NP_001335013.1:n.2933+108G=
NM_182643.3:c.4466+108G= MANE Select NP_872584.2:n.4466+108G=
NM_001316668.2:c.3257+108G= NP_001303597.1:n.3257+108G=
NM_001348081.2:c.4466+108G= NP_001335010.1:n.4466+108G=
NM_001348082.2:c.2933+108G= NP_001335011.1:n.2933+108G=
NM_001348084.2:c.2933+108G= NP_001335013.1:n.2933+108G=
NM_006094.5:c.3155+108G= NP_006085.2:n.3155+108G=
NM_001164271.2:c.2933+108G= NP_001157743.1:n.2933+108G=