Canonical Allele Identifier: CA1764989955

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13201165C= , CM000670.2:g.13201165C=	GRCh38
NC_000008.10:g.13058674C= , CM000670.1:g.13058674C=	GRCh37
NC_000008.9:g.13103045C=	NCBI36
NG_015998.1:g.318756G=
NG_015998.2:g.408441G=

Transcript Alleles

HGVS	Amino-acid Change
NM_182643.3:c.1349-85508G= MANE Select	NP_872584.2:n.1349-85508G=
ENST00000276297.9:c.1349-85508G= MANE Select	ENSP00000276297.4:n.1349-85508G=
NM_001316668.1:c.139+75097G=	NP_001303597.1:n.139+75097G=
NM_001316668.2:c.139+75097G=	NP_001303597.1:n.139+75097G=
NM_001348081.1:c.1349-85508G=	NP_001335010.1:n.1349-85508G=
NM_001348081.2:c.1349-85508G=	NP_001335010.1:n.1349-85508G=
NM_001348082.1:c.-103-85508G=	NP_001335011.1:n.-103-85508G=
NM_001348082.2:c.-103-85508G=	NP_001335011.1:n.-103-85508G=
NM_001348083.1:c.-186+75530G=	NP_001335012.1:n.-186+75530G=
NM_182643.2:c.1349-85508G=	NP_872584.2:n.1349-85508G=
ENST00000276297.8:c.1349-85508G=	ENSP00000276297.4:n.1349-85508G=
ENST00000503161.6:c.-238+75530G=	ENSP00000429537.1:n.-238+75530G=
ENST00000509922.5:n.90+75530G=
ENST00000512044.6:c.139+75097G=	ENSP00000422595.2:n.139+75097G=
XM_005273374.1:c.1349-85508G=	XP_005273431.1:n.1349-85508G=