Canonical Allele Identifier: CA3156051440
Community Standard Title: NM_182643.3(DLC1):c.1024-1408G>T
Gene: DLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.13403027C>A , CM000670.2:g.13403027C>A GRCh38
NC_000008.10:g.13260536C>A , CM000670.1:g.13260536C>A GRCh37
NC_000008.9:g.13304907C>A NCBI36
NG_015998.1:g.116894G>T
NG_015998.2:g.206579G>T

Transcript Alleles

HGVS Amino-acid Change
NM_182643.3:c.1024-1408G>T MANE Select NP_872584.2:n.1024-1408G>T
ENST00000276297.9:c.1024-1408G>T MANE Select ENSP00000276297.4:n.1024-1408G>T
NM_001348081.1:c.1024-1408G>T NP_001335010.1:n.1024-1408G>T
NM_001348081.2:c.1024-1408G>T NP_001335010.1:n.1024-1408G>T
NM_001348082.1:c.-428-1408G>T NP_001335011.1:n.-428-1408G>T
NM_001348082.2:c.-428-1408G>T NP_001335011.1:n.-428-1408G>T
NM_024767.3:c.1024-1408G>T NP_079043.3:n.1024-1408G>T
NM_024767.4:c.1024-1408G>T NP_079043.3:n.1024-1408G>T
NM_024767.5:c.1024-1408G>T NP_079043.3:n.1024-1408G>T
NM_182643.2:c.1024-1408G>T NP_872584.2:n.1024-1408G>T
ENST00000276297.8:c.1024-1408G>T ENSP00000276297.4:n.1024-1408G>T
ENST00000316609.9:c.1024-1408G>T ENSP00000321034.5:n.1024-1408G>T
ENST00000511869.1:c.1024-1408G>T ENSP00000425878.1:n.1024-1408G>T
XM_005273374.1:c.1024-1408G>T XP_005273431.1:n.1024-1408G>T