Canonical Allele Identifier: CA4639404

Gene: DLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13499298C>T , CM000670.2:g.13499298C>T	GRCh38
NC_000008.10:g.13356807C>T , CM000670.1:g.13356807C>T	GRCh37
NC_000008.9:g.13401178C>T	NCBI36
NG_015998.1:g.20623G>A
NG_015998.2:g.110308G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.774G>A MANE Select	ENSP00000276297.4:p.Leu258=
ENST00000276297.8:c.774G>A	ENSP00000276297.4:p.Leu258=
ENST00000316609.9:c.774G>A	ENSP00000321034.5:p.Leu258=
ENST00000511869.1:c.774G>A	ENSP00000425878.1:p.Leu258=
NM_024767.3:c.774G>A	NP_079043.3:p.Leu258=
NM_182643.2:c.774G>A	NP_872584.2:p.Leu258=
XM_005273374.1:c.774G>A	XP_005273431.1:p.Leu258=
NM_001348081.1:c.774G>A	NP_001335010.1:p.Leu258=
NM_001348082.1:c.-678G>A	NP_001335011.1:n.-678G>A
NM_182643.3:c.774G>A MANE Select	NP_872584.2:p.Leu258=
NM_001348081.2:c.774G>A	NP_001335010.1:p.Leu258=
NM_001348082.2:c.-678G>A	NP_001335011.1:n.-678G>A
NM_024767.4:c.774G>A	NP_079043.3:p.Leu258=
NM_024767.5:c.774G>A	NP_079043.3:p.Leu258=