Canonical Allele Identifier: CA2838366338

Gene: DCP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1956384A>G , CM000674.2:g.1956384A>G	GRCh38
NC_000012.11:g.2065550A>G , CM000674.1:g.2065550A>G	GRCh37
NC_000012.10:g.1935811A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280665.11:c.523-824T>C MANE Select	ENSP00000280665.6:n.523-824T>C
ENST00000280665.10:c.523-824T>C	ENSP00000280665.6:n.523-824T>C
ENST00000536665.5:n.199-824T>C
ENST00000540622.1:c.145-824T>C	ENSP00000444374.1:n.145-824T>C
ENST00000541700.5:n.437-3096T>C
ENST00000543381.5:c.*289-824T>C	ENSP00000445011.1:n.*289-824T>C
NM_152640.3:c.523-824T>C	NP_689853.3:n.523-824T>C
XM_011520927.1:c.217-824T>C	XP_011519229.1:n.217-824T>C
XM_011520928.1:c.145-824T>C	XP_011519230.1:n.145-824T>C
NM_152640.4:c.523-824T>C	NP_689853.3:n.523-824T>C
NR_135060.1:n.753-824T>C
XM_011520927.3:c.217-824T>C	XP_011519229.1:n.217-824T>C
NM_152640.5:c.523-824T>C MANE Select	NP_689853.3:n.523-824T>C
NR_135060.2:n.675-824T>C