Canonical Allele Identifier: CA2581064179

Gene: DCP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1947197C>A , CM000674.2:g.1947197C>A	GRCh38
NC_000012.11:g.2056363C>A , CM000674.1:g.2056363C>A	GRCh37
NC_000012.10:g.1926624C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152640.5:c.1774-911G>T MANE Select	NP_689853.3:n.1774-911G>T
ENST00000280665.11:c.1774-911G>T MANE Select	ENSP00000280665.6:n.1774-911G>T
NM_152640.3:c.1774-911G>T	NP_689853.3:n.1774-911G>T
NM_152640.4:c.1774-911G>T	NP_689853.3:n.1774-911G>T
NR_135060.1:n.2004-911G>T
NR_135060.2:n.1926-911G>T
ENST00000280665.10:c.1774-911G>T	ENSP00000280665.6:n.1774-911G>T
ENST00000543381.5:c.*1540-911G>T	ENSP00000445011.1:n.*1540-911G>T
XM_011520927.1:c.1468-911G>T	XP_011519229.1:n.1468-911G>T
XM_011520927.3:c.1468-911G>T	XP_011519229.1:n.1468-911G>T
XM_011520928.1:c.1396-911G>T	XP_011519230.1:n.1396-911G>T