Canonical Allele Identifier: CA172240040
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13133431C>T , CM000670.2:g.13133431C>T GRCh38
NC_000008.10:g.12990940C>T , CM000670.1:g.12990940C>T GRCh37
NC_000008.9:g.13035311C>T NCBI36
NG_015998.1:g.386490G>A
NG_015998.2:g.476175G>A

Transcript Alleles

HGVS Amino-acid Change
NM_182643.3:c.1349-17774G>A MANE Select NP_872584.2:n.1349-17774G>A
ENST00000276297.9:c.1349-17774G>A MANE Select ENSP00000276297.4:n.1349-17774G>A
NM_001316668.1:c.140-17774G>A NP_001303597.1:n.140-17774G>A
NM_001316668.2:c.140-17774G>A NP_001303597.1:n.140-17774G>A
NM_001348081.1:c.1349-17774G>A NP_001335010.1:n.1349-17774G>A
NM_001348081.2:c.1349-17774G>A NP_001335010.1:n.1349-17774G>A
NM_001348082.1:c.-103-17774G>A NP_001335011.1:n.-103-17774G>A
NM_001348082.2:c.-103-17774G>A NP_001335011.1:n.-103-17774G>A
NM_001348083.1:c.-185-17774G>A NP_001335012.1:n.-185-17774G>A
NM_182643.2:c.1349-17774G>A NP_872584.2:n.1349-17774G>A
ENST00000276297.8:c.1349-17774G>A ENSP00000276297.4:n.1349-17774G>A
ENST00000358919.6:c.-451G>A ENSP00000351797.2:n.-451G>A
ENST00000503161.6:c.-237-17774G>A ENSP00000429537.1:n.-237-17774G>A
ENST00000509922.5:n.91-17774G>A
ENST00000512044.6:c.140-17774G>A ENSP00000422595.2:n.140-17774G>A
XM_005273374.1:c.1349-17774G>A XP_005273431.1:n.1349-17774G>A