Canonical Allele Identifier: CA4638469

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13098570C>T , CM000670.2:g.13098570C>T	GRCh38
NC_000008.10:g.12956079C>T , CM000670.1:g.12956079C>T	GRCh37
NC_000008.9:g.13000450C>T	NCBI36
NG_015998.1:g.421351G>A
NG_015998.2:g.511036G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.2996G>A MANE Select	ENSP00000276297.4:p.Arg999Gln
ENST00000276297.8:c.2996G>A	ENSP00000276297.4:p.Arg999Gln
ENST00000358919.6:c.1685G>A	ENSP00000351797.2:p.Arg562Gln
ENST00000510250.2:n.1565G>A
ENST00000512044.6:c.1787G>A	ENSP00000422595.2:p.Arg596Gln
ENST00000520226.5:c.1463G>A	ENSP00000428028.1:p.Arg488Gln
NM_001164271.1:c.1463G>A	NP_001157743.1:p.Arg488Gln
NM_001316668.1:c.1787G>A	NP_001303597.1:p.Arg596Gln
NM_006094.4:c.1685G>A	NP_006085.2:p.Arg562Gln
NM_182643.2:c.2996G>A	NP_872584.2:p.Arg999Gln
XM_005273374.1:c.2996G>A	XP_005273431.1:p.Arg999Gln
NM_001348081.1:c.2996G>A	NP_001335010.1:p.Arg999Gln
NM_001348082.1:c.1463G>A	NP_001335011.1:p.Arg488Gln
NM_001348083.1:c.1463G>A	NP_001335012.1:p.Arg488Gln
NM_001348084.1:c.1463G>A	NP_001335013.1:p.Arg488Gln
NM_182643.3:c.2996G>A MANE Select	NP_872584.2:p.Arg999Gln
NM_001316668.2:c.1787G>A	NP_001303597.1:p.Arg596Gln
NM_001348081.2:c.2996G>A	NP_001335010.1:p.Arg999Gln
NM_001348082.2:c.1463G>A	NP_001335011.1:p.Arg488Gln
NM_001348084.2:c.1463G>A	NP_001335013.1:p.Arg488Gln
NM_006094.5:c.1685G>A	NP_006085.2:p.Arg562Gln
NM_001164271.2:c.1463G>A	NP_001157743.1:p.Arg488Gln