Canonical Allele Identifier: CA4638159
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13091354C>T , CM000670.2:g.13091354C>T GRCh38
NC_000008.10:g.12948863C>T , CM000670.1:g.12948863C>T GRCh37
NC_000008.9:g.12993234C>T NCBI36
NG_015998.1:g.428567G>A
NG_015998.2:g.518252G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276297.9:c.3819G>A MANE Select ENSP00000276297.4:p.Leu1273=
ENST00000276297.8:c.3819G>A ENSP00000276297.4:p.Leu1273=
ENST00000358919.6:c.2508G>A ENSP00000351797.2:p.Leu836=
ENST00000510318.5:n.1004G>A
ENST00000512044.6:c.2610G>A ENSP00000422595.2:p.Leu870=
ENST00000520226.5:c.2286G>A ENSP00000428028.1:p.Leu762=
NM_001164271.1:c.2286G>A NP_001157743.1:p.Leu762=
NM_001316668.1:c.2610G>A NP_001303597.1:p.Leu870=
NM_006094.4:c.2508G>A NP_006085.2:p.Leu836=
NM_182643.2:c.3819G>A NP_872584.2:p.Leu1273=
XM_005273374.1:c.3819G>A XP_005273431.1:p.Leu1273=
NM_001348081.1:c.3819G>A NP_001335010.1:p.Leu1273=
NM_001348082.1:c.2286G>A NP_001335011.1:p.Leu762=
NM_001348083.1:c.2286G>A NP_001335012.1:p.Leu762=
NM_001348084.1:c.2286G>A NP_001335013.1:p.Leu762=
NM_182643.3:c.3819G>A MANE Select NP_872584.2:p.Leu1273=
NM_001316668.2:c.2610G>A NP_001303597.1:p.Leu870=
NM_001348081.2:c.3819G>A NP_001335010.1:p.Leu1273=
NM_001348082.2:c.2286G>A NP_001335011.1:p.Leu762=
NM_001348084.2:c.2286G>A NP_001335013.1:p.Leu762=
NM_006094.5:c.2508G>A NP_006085.2:p.Leu836=
NM_001164271.2:c.2286G>A NP_001157743.1:p.Leu762=