Canonical Allele Identifier: CA1765041711
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13318843A= , CM000670.2:g.13318843A= GRCh38
NC_000008.10:g.13176352A= , CM000670.1:g.13176352A= GRCh37
NC_000008.9:g.13220723A= NCBI36
NG_015998.1:g.201078T=
NG_015998.2:g.290763T=

Transcript Alleles

HGVS Amino-acid change
ENST00000276297.9:c.1315-13541T= MANE Select ENSP00000276297.4:n.1315-13541T=
ENST00000276297.8:c.1315-13541T= ENSP00000276297.4:n.1315-13541T=
ENST00000316609.9:c.1315-13541T= ENSP00000321034.5:n.1315-13541T=
ENST00000511869.1:c.1315-13541T= ENSP00000425878.1:n.1315-13541T=
NM_024767.3:c.1315-13541T= NP_079043.3:n.1315-13541T=
NM_182643.2:c.1315-13541T= NP_872584.2:n.1315-13541T=
XM_005273374.1:c.1315-13541T= XP_005273431.1:n.1315-13541T=
NM_001348081.1:c.1315-13541T= NP_001335010.1:n.1315-13541T=
NM_001348082.1:c.-137-13541T= NP_001335011.1:n.-137-13541T=
NM_182643.3:c.1315-13541T= MANE Select NP_872584.2:n.1315-13541T=
NM_001348081.2:c.1315-13541T= NP_001335010.1:n.1315-13541T=
NM_001348082.2:c.-137-13541T= NP_001335011.1:n.-137-13541T=
NM_024767.4:c.1315-13541T= NP_079043.3:n.1315-13541T=
NM_024767.5:c.1315-13541T= NP_079043.3:n.1315-13541T=