Canonical Allele Identifier: CA1765042135

Gene: DLC1

Linked Data

• dbSNP Id: rs562860637

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.13319204C>T , CM000670.2:g.13319204C>T	GRCh38
NC_000008.10:g.13176713C>T , CM000670.1:g.13176713C>T	GRCh37
NC_000008.9:g.13221084C>T	NCBI36
NG_015998.1:g.200717G>A
NG_015998.2:g.290402G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276297.9:c.1315-13902G>A MANE Select	ENSP00000276297.4:n.1315-13902G>A
ENST00000276297.8:c.1315-13902G>A	ENSP00000276297.4:n.1315-13902G>A
ENST00000316609.9:c.1315-13902G>A	ENSP00000321034.5:n.1315-13902G>A
ENST00000511869.1:c.1315-13902G>A	ENSP00000425878.1:n.1315-13902G>A
NM_024767.3:c.1315-13902G>A	NP_079043.3:n.1315-13902G>A
NM_182643.2:c.1315-13902G>A	NP_872584.2:n.1315-13902G>A
XM_005273374.1:c.1315-13902G>A	XP_005273431.1:n.1315-13902G>A
NM_001348081.1:c.1315-13902G>A	NP_001335010.1:n.1315-13902G>A
NM_001348082.1:c.-137-13902G>A	NP_001335011.1:n.-137-13902G>A
NM_182643.3:c.1315-13902G>A MANE Select	NP_872584.2:n.1315-13902G>A
NM_001348081.2:c.1315-13902G>A	NP_001335010.1:n.1315-13902G>A
NM_001348082.2:c.-137-13902G>A	NP_001335011.1:n.-137-13902G>A
NM_024767.4:c.1315-13902G>A	NP_079043.3:n.1315-13902G>A
NM_024767.5:c.1315-13902G>A	NP_079043.3:n.1315-13902G>A