Canonical Allele Identifier: CA172181347

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13088343G>A , CM000670.2:g.13088343G>A	GRCh38
NC_000008.10:g.12945852G>A , CM000670.1:g.12945852G>A	GRCh37
NC_000008.9:g.12990223G>A	NCBI36
NG_015998.1:g.431578C>T
NG_015998.2:g.521263C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_182643.3:c.4292+144C>T MANE Select	NP_872584.2:n.4292+144C>T
ENST00000276297.9:c.4292+144C>T MANE Select	ENSP00000276297.4:n.4292+144C>T
NM_001164271.1:c.2759+144C>T	NP_001157743.1:n.2759+144C>T
NM_001164271.2:c.2759+144C>T	NP_001157743.1:n.2759+144C>T
NM_001316668.1:c.3083+144C>T	NP_001303597.1:n.3083+144C>T
NM_001316668.2:c.3083+144C>T	NP_001303597.1:n.3083+144C>T
NM_001348081.1:c.4292+144C>T	NP_001335010.1:n.4292+144C>T
NM_001348081.2:c.4292+144C>T	NP_001335010.1:n.4292+144C>T
NM_001348082.1:c.2759+144C>T	NP_001335011.1:n.2759+144C>T
NM_001348082.2:c.2759+144C>T	NP_001335011.1:n.2759+144C>T
NM_001348083.1:c.2759+144C>T	NP_001335012.1:n.2759+144C>T
NM_001348084.1:c.2759+144C>T	NP_001335013.1:n.2759+144C>T
NM_001348084.2:c.2759+144C>T	NP_001335013.1:n.2759+144C>T
NM_006094.4:c.2981+144C>T	NP_006085.2:n.2981+144C>T
NM_006094.5:c.2981+144C>T	NP_006085.2:n.2981+144C>T
NM_182643.2:c.4292+144C>T	NP_872584.2:n.4292+144C>T
ENST00000276297.8:c.4292+144C>T	ENSP00000276297.4:n.4292+144C>T
ENST00000358919.6:c.2981+144C>T	ENSP00000351797.2:n.2981+144C>T
ENST00000510318.5:n.1477+144C>T
ENST00000512044.6:c.3083+144C>T	ENSP00000422595.2:n.3083+144C>T
ENST00000520226.5:c.2759+144C>T	ENSP00000428028.1:n.2759+144C>T
ENST00000521730.1:n.253+144C>T
XM_005273374.1:c.4292+144C>T	XP_005273431.1:n.4292+144C>T