Canonical Allele Identifier: CA3056649317

Gene: DCP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1947022T>C , CM000674.2:g.1947022T>C	GRCh38
NC_000012.11:g.2056188T>C , CM000674.1:g.2056188T>C	GRCh37
NC_000012.10:g.1926449T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152640.5:c.1774-736A>G MANE Select	NP_689853.3:n.1774-736A>G
ENST00000280665.11:c.1774-736A>G MANE Select	ENSP00000280665.6:n.1774-736A>G
NM_152640.3:c.1774-736A>G	NP_689853.3:n.1774-736A>G
NM_152640.4:c.1774-736A>G	NP_689853.3:n.1774-736A>G
NR_135060.1:n.2004-736A>G
NR_135060.2:n.1926-736A>G
ENST00000280665.10:c.1774-736A>G	ENSP00000280665.6:n.1774-736A>G
ENST00000543381.5:c.*1540-736A>G	ENSP00000445011.1:n.*1540-736A>G
XM_011520927.1:c.1468-736A>G	XP_011519229.1:n.1468-736A>G
XM_011520927.3:c.1468-736A>G	XP_011519229.1:n.1468-736A>G
XM_011520928.1:c.1396-736A>G	XP_011519230.1:n.1396-736A>G