Canonical Allele Identifier: CA2838376341

Gene: DCP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1948987G>T , CM000674.2:g.1948987G>T	GRCh38
NC_000012.11:g.2058153G>T , CM000674.1:g.2058153G>T	GRCh37
NC_000012.10:g.1928414G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280665.11:c.1773+99C>A MANE Select	ENSP00000280665.6:n.1773+99C>A
ENST00000280665.10:c.1773+99C>A	ENSP00000280665.6:n.1773+99C>A
ENST00000543381.5:c.*1539+99C>A	ENSP00000445011.1:n.*1539+99C>A
NM_152640.3:c.1773+99C>A	NP_689853.3:n.1773+99C>A
XM_011520927.1:c.1467+99C>A	XP_011519229.1:n.1467+99C>A
XM_011520928.1:c.1395+99C>A	XP_011519230.1:n.1395+99C>A
NM_152640.4:c.1773+99C>A	NP_689853.3:n.1773+99C>A
NR_135060.1:n.2003+99C>A
XM_011520927.3:c.1467+99C>A	XP_011519229.1:n.1467+99C>A
NM_152640.5:c.1773+99C>A MANE Select	NP_689853.3:n.1773+99C>A
NR_135060.2:n.1925+99C>A