Canonical Allele Identifier: CA2339994972

Gene: DBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633495G= , CM000681.2:g.48633495G=	GRCh38
NC_000019.9:g.49136752G= , CM000681.1:g.49136752G=	GRCh37
NC_000019.8:g.53828564G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.711C= MANE Select	ENSP00000222122.4:p.Pro237=
ENST00000222122.9:c.711C=	ENSP00000222122.4:p.Pro237=
ENST00000593500.1:c.105C=	ENSP00000471220.1:p.Pro35=
ENST00000594723.1:n.2954C=
ENST00000599385.5:c.105C=	ENSP00000469426.1:p.Pro35=
ENST00000601104.1:c.711C=	ENSP00000469291.1:p.Pro237=
NM_001352.4:c.711C=	NP_001343.2:p.Pro237=
XM_017026388.2:c.282C=	XP_016881877.1:p.Pro94=
XR_243907.4:n.1616C=
NM_001352.5:c.711C= MANE Select	NP_001343.2:p.Pro237=