Canonical Allele Identifier: CA1764930141

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13099462T= , CM000670.2:g.13099462T=	GRCh38
NC_000008.10:g.12956971T= , CM000670.1:g.12956971T=	GRCh37
NC_000008.9:g.13001342T=	NCBI36
NG_015998.1:g.420459A=
NG_015998.2:g.510144A=

Transcript Alleles

HGVS	Amino-acid Change
NM_182643.3:c.2875A= MANE Select	NP_872584.2:p.Thr959=
ENST00000276297.9:c.2875A= MANE Select	ENSP00000276297.4:p.Thr959=
NM_001164271.1:c.1342A=	NP_001157743.1:p.Thr448=
NM_001164271.2:c.1342A=	NP_001157743.1:p.Thr448=
NM_001316668.1:c.1666A=	NP_001303597.1:p.Thr556=
NM_001316668.2:c.1666A=	NP_001303597.1:p.Thr556=
NM_001348081.1:c.2875A=	NP_001335010.1:p.Thr959=
NM_001348081.2:c.2875A=	NP_001335010.1:p.Thr959=
NM_001348082.1:c.1342A=	NP_001335011.1:p.Thr448=
NM_001348082.2:c.1342A=	NP_001335011.1:p.Thr448=
NM_001348083.1:c.1342A=	NP_001335012.1:p.Thr448=
NM_001348084.1:c.1342A=	NP_001335013.1:p.Thr448=
NM_001348084.2:c.1342A=	NP_001335013.1:p.Thr448=
NM_006094.4:c.1564A=	NP_006085.2:p.Thr522=
NM_006094.5:c.1564A=	NP_006085.2:p.Thr522=
NM_182643.2:c.2875A=	NP_872584.2:p.Thr959=
ENST00000276297.8:c.2875A=	ENSP00000276297.4:p.Thr959=
ENST00000358919.6:c.1564A=	ENSP00000351797.2:p.Thr522=
ENST00000510250.2:n.1444A=
ENST00000512044.6:c.1666A=	ENSP00000422595.2:p.Thr556=
ENST00000520226.5:c.1342A=	ENSP00000428028.1:p.Thr448=
XM_005273374.1:c.2875A=	XP_005273431.1:p.Thr959=