Canonical Allele Identifier: CA4638634
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13099944C>T , CM000670.2:g.13099944C>T GRCh38
NC_000008.10:g.12957453C>T , CM000670.1:g.12957453C>T GRCh37
NC_000008.9:g.13001824C>T NCBI36
NG_015998.1:g.419977G>A
NG_015998.2:g.509662G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276297.9:c.2393G>A MANE Select ENSP00000276297.4:p.Arg798His
ENST00000276297.8:c.2393G>A ENSP00000276297.4:p.Arg798His
ENST00000358919.6:c.1082G>A ENSP00000351797.2:p.Arg361His
ENST00000510250.2:n.962G>A
ENST00000512044.6:c.1184G>A ENSP00000422595.2:p.Arg395His
ENST00000520226.5:c.860G>A ENSP00000428028.1:p.Arg287His
NM_001164271.1:c.860G>A NP_001157743.1:p.Arg287His
NM_001316668.1:c.1184G>A NP_001303597.1:p.Arg395His
NM_006094.4:c.1082G>A NP_006085.2:p.Arg361His
NM_182643.2:c.2393G>A NP_872584.2:p.Arg798His
XM_005273374.1:c.2393G>A XP_005273431.1:p.Arg798His
NM_001348081.1:c.2393G>A NP_001335010.1:p.Arg798His
NM_001348082.1:c.860G>A NP_001335011.1:p.Arg287His
NM_001348083.1:c.860G>A NP_001335012.1:p.Arg287His
NM_001348084.1:c.860G>A NP_001335013.1:p.Arg287His
NM_182643.3:c.2393G>A MANE Select NP_872584.2:p.Arg798His
NM_001316668.2:c.1184G>A NP_001303597.1:p.Arg395His
NM_001348081.2:c.2393G>A NP_001335010.1:p.Arg798His
NM_001348082.2:c.860G>A NP_001335011.1:p.Arg287His
NM_001348084.2:c.860G>A NP_001335013.1:p.Arg287His
NM_006094.5:c.1082G>A NP_006085.2:p.Arg361His
NM_001164271.2:c.860G>A NP_001157743.1:p.Arg287His