Canonical Allele Identifier: CA2339994917

Gene: DBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633389T= , CM000681.2:g.48633389T=	GRCh38
NC_000019.9:g.49136646T= , CM000681.1:g.49136646T=	GRCh37
NC_000019.8:g.53828458T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+55A= MANE Select	ENSP00000222122.4:n.762+55A=
ENST00000222122.9:c.762+55A=	ENSP00000222122.4:n.762+55A=
ENST00000593500.1:c.156+55A=	ENSP00000471220.1:n.156+55A=
ENST00000594723.1:n.3060A=
ENST00000599385.5:c.156+55A=	ENSP00000469426.1:n.156+55A=
ENST00000601104.1:c.*28A=	ENSP00000469291.1:n.*28A=
NM_001352.4:c.762+55A=	NP_001343.2:n.762+55A=
XM_017026388.2:c.333+55A=	XP_016881877.1:n.333+55A=
XR_243907.4:n.1667+55A=
NM_001352.5:c.762+55A= MANE Select	NP_001343.2:n.762+55A=