Canonical Allele Identifier: CA4638253

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13092743G>T , CM000670.2:g.13092743G>T	GRCh38
NC_000008.10:g.12950252G>T , CM000670.1:g.12950252G>T	GRCh37
NC_000008.9:g.12994623G>T	NCBI36
NG_015998.1:g.427178C>A
NG_015998.2:g.516863C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.3609C>A MANE Select	ENSP00000276297.4:p.Thr1203=
ENST00000276297.8:c.3609C>A	ENSP00000276297.4:p.Thr1203=
ENST00000358919.6:c.2298C>A	ENSP00000351797.2:p.Thr766=
ENST00000510318.5:n.794C>A
ENST00000512044.6:c.2400C>A	ENSP00000422595.2:p.Thr800=
ENST00000520226.5:c.2076C>A	ENSP00000428028.1:p.Thr692=
NM_001164271.1:c.2076C>A	NP_001157743.1:p.Thr692=
NM_001316668.1:c.2400C>A	NP_001303597.1:p.Thr800=
NM_006094.4:c.2298C>A	NP_006085.2:p.Thr766=
NM_182643.2:c.3609C>A	NP_872584.2:p.Thr1203=
XM_005273374.1:c.3609C>A	XP_005273431.1:p.Thr1203=
NM_001348081.1:c.3609C>A	NP_001335010.1:p.Thr1203=
NM_001348082.1:c.2076C>A	NP_001335011.1:p.Thr692=
NM_001348083.1:c.2076C>A	NP_001335012.1:p.Thr692=
NM_001348084.1:c.2076C>A	NP_001335013.1:p.Thr692=
NM_182643.3:c.3609C>A MANE Select	NP_872584.2:p.Thr1203=
NM_001316668.2:c.2400C>A	NP_001303597.1:p.Thr800=
NM_001348081.2:c.3609C>A	NP_001335010.1:p.Thr1203=
NM_001348082.2:c.2076C>A	NP_001335011.1:p.Thr692=
NM_001348084.2:c.2076C>A	NP_001335013.1:p.Thr692=
NM_006094.5:c.2298C>A	NP_006085.2:p.Thr766=
NM_001164271.2:c.2076C>A	NP_001157743.1:p.Thr692=