Canonical Allele Identifier: CA4638786
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13100492G>A , CM000670.2:g.13100492G>A GRCh38
NC_000008.10:g.12958001G>A , CM000670.1:g.12958001G>A GRCh37
NC_000008.9:g.13002372G>A NCBI36
NG_015998.1:g.419429C>T
NG_015998.2:g.509114C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276297.9:c.1845C>T MANE Select ENSP00000276297.4:p.Thr615=
ENST00000276297.8:c.1845C>T ENSP00000276297.4:p.Thr615=
ENST00000358919.6:c.534C>T ENSP00000351797.2:p.Thr178=
ENST00000510250.2:n.414C>T
ENST00000512044.6:c.636C>T ENSP00000422595.2:p.Thr212=
ENST00000520226.5:c.312C>T ENSP00000428028.1:p.Thr104=
NM_001164271.1:c.312C>T NP_001157743.1:p.Thr104=
NM_001316668.1:c.636C>T NP_001303597.1:p.Thr212=
NM_006094.4:c.534C>T NP_006085.2:p.Thr178=
NM_182643.2:c.1845C>T NP_872584.2:p.Thr615=
XM_005273374.1:c.1845C>T XP_005273431.1:p.Thr615=
NM_001348081.1:c.1845C>T NP_001335010.1:p.Thr615=
NM_001348082.1:c.312C>T NP_001335011.1:p.Thr104=
NM_001348083.1:c.312C>T NP_001335012.1:p.Thr104=
NM_001348084.1:c.312C>T NP_001335013.1:p.Thr104=
NM_182643.3:c.1845C>T MANE Select NP_872584.2:p.Thr615=
NM_001316668.2:c.636C>T NP_001303597.1:p.Thr212=
NM_001348081.2:c.1845C>T NP_001335010.1:p.Thr615=
NM_001348082.2:c.312C>T NP_001335011.1:p.Thr104=
NM_001348084.2:c.312C>T NP_001335013.1:p.Thr104=
NM_006094.5:c.534C>T NP_006085.2:p.Thr178=
NM_001164271.2:c.312C>T NP_001157743.1:p.Thr104=