Canonical Allele Identifier: CA16326740

Gene: DLC1

Linked Data

• dbSNP Id: rs289585
• gnomAD v2: 8-13260536-C-T
• gnomAD v3: 8-13403027-C-T
• gnomAD v4: 8-13403027-C-T
• MyVariant Identifiers: chr8:g.13260536C>T (hg19) ; chr8:g.13403027C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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