Canonical Allele Identifier: CA1765041784
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13318915C= , CM000670.2:g.13318915C= GRCh38
NC_000008.10:g.13176424C= , CM000670.1:g.13176424C= GRCh37
NC_000008.9:g.13220795C= NCBI36
NG_015998.1:g.201006G=
NG_015998.2:g.290691G=

Transcript Alleles

HGVS Amino-acid change
ENST00000276297.9:c.1315-13613G= MANE Select ENSP00000276297.4:n.1315-13613G=
ENST00000276297.8:c.1315-13613G= ENSP00000276297.4:n.1315-13613G=
ENST00000316609.9:c.1315-13613G= ENSP00000321034.5:n.1315-13613G=
ENST00000511869.1:c.1315-13613G= ENSP00000425878.1:n.1315-13613G=
NM_024767.3:c.1315-13613G= NP_079043.3:n.1315-13613G=
NM_182643.2:c.1315-13613G= NP_872584.2:n.1315-13613G=
XM_005273374.1:c.1315-13613G= XP_005273431.1:n.1315-13613G=
NM_001348081.1:c.1315-13613G= NP_001335010.1:n.1315-13613G=
NM_001348082.1:c.-137-13613G= NP_001335011.1:n.-137-13613G=
NM_182643.3:c.1315-13613G= MANE Select NP_872584.2:n.1315-13613G=
NM_001348081.2:c.1315-13613G= NP_001335010.1:n.1315-13613G=
NM_001348082.2:c.-137-13613G= NP_001335011.1:n.-137-13613G=
NM_024767.4:c.1315-13613G= NP_079043.3:n.1315-13613G=
NM_024767.5:c.1315-13613G= NP_079043.3:n.1315-13613G=