Canonical Allele Identifier: CA4638688

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13100138G>A , CM000670.2:g.13100138G>A	GRCh38
NC_000008.10:g.12957647G>A , CM000670.1:g.12957647G>A	GRCh37
NC_000008.9:g.13002018G>A	NCBI36
NG_015998.1:g.419783C>T
NG_015998.2:g.509468C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.2199C>T MANE Select	ENSP00000276297.4:p.Ser733=
ENST00000276297.8:c.2199C>T	ENSP00000276297.4:p.Ser733=
ENST00000358919.6:c.888C>T	ENSP00000351797.2:p.Ser296=
ENST00000510250.2:n.768C>T
ENST00000512044.6:c.990C>T	ENSP00000422595.2:p.Ser330=
ENST00000520226.5:c.666C>T	ENSP00000428028.1:p.Ser222=
NM_001164271.1:c.666C>T	NP_001157743.1:p.Ser222=
NM_001316668.1:c.990C>T	NP_001303597.1:p.Ser330=
NM_006094.4:c.888C>T	NP_006085.2:p.Ser296=
NM_182643.2:c.2199C>T	NP_872584.2:p.Ser733=
XM_005273374.1:c.2199C>T	XP_005273431.1:p.Ser733=
NM_001348081.1:c.2199C>T	NP_001335010.1:p.Ser733=
NM_001348082.1:c.666C>T	NP_001335011.1:p.Ser222=
NM_001348083.1:c.666C>T	NP_001335012.1:p.Ser222=
NM_001348084.1:c.666C>T	NP_001335013.1:p.Ser222=
NM_182643.3:c.2199C>T MANE Select	NP_872584.2:p.Ser733=
NM_001316668.2:c.990C>T	NP_001303597.1:p.Ser330=
NM_001348081.2:c.2199C>T	NP_001335010.1:p.Ser733=
NM_001348082.2:c.666C>T	NP_001335011.1:p.Ser222=
NM_001348084.2:c.666C>T	NP_001335013.1:p.Ser222=
NM_006094.5:c.888C>T	NP_006085.2:p.Ser296=
NM_001164271.2:c.666C>T	NP_001157743.1:p.Ser222=