Canonical Allele Identifier: CA1765042121

Gene: DLC1

Linked Data

• dbSNP Id: rs1832984118

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13319195A>C , CM000670.2:g.13319195A>C	GRCh38
NC_000008.10:g.13176704A>C , CM000670.1:g.13176704A>C	GRCh37
NC_000008.9:g.13221075A>C	NCBI36
NG_015998.1:g.200726T>G
NG_015998.2:g.290411T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.1315-13893T>G MANE Select	ENSP00000276297.4:n.1315-13893T>G
ENST00000276297.8:c.1315-13893T>G	ENSP00000276297.4:n.1315-13893T>G
ENST00000316609.9:c.1315-13893T>G	ENSP00000321034.5:n.1315-13893T>G
ENST00000511869.1:c.1315-13893T>G	ENSP00000425878.1:n.1315-13893T>G
NM_024767.3:c.1315-13893T>G	NP_079043.3:n.1315-13893T>G
NM_182643.2:c.1315-13893T>G	NP_872584.2:n.1315-13893T>G
XM_005273374.1:c.1315-13893T>G	XP_005273431.1:n.1315-13893T>G
NM_001348081.1:c.1315-13893T>G	NP_001335010.1:n.1315-13893T>G
NM_001348082.1:c.-137-13893T>G	NP_001335011.1:n.-137-13893T>G
NM_182643.3:c.1315-13893T>G MANE Select	NP_872584.2:n.1315-13893T>G
NM_001348081.2:c.1315-13893T>G	NP_001335010.1:n.1315-13893T>G
NM_001348082.2:c.-137-13893T>G	NP_001335011.1:n.-137-13893T>G
NM_024767.4:c.1315-13893T>G	NP_079043.3:n.1315-13893T>G
NM_024767.5:c.1315-13893T>G	NP_079043.3:n.1315-13893T>G