Canonical Allele Identifier: CA2339994971

Gene: DBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633490G= , CM000681.2:g.48633490G=	GRCh38
NC_000019.9:g.49136747G= , CM000681.1:g.49136747G=	GRCh37
NC_000019.8:g.53828559G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.716C= MANE Select	ENSP00000222122.4:p.Pro239=
ENST00000222122.9:c.716C=	ENSP00000222122.4:p.Pro239=
ENST00000593500.1:c.110C=	ENSP00000471220.1:p.Pro37=
ENST00000594723.1:n.2959C=
ENST00000599385.5:c.110C=	ENSP00000469426.1:p.Pro37=
ENST00000601104.1:c.716C=	ENSP00000469291.1:p.Pro239=
NM_001352.4:c.716C=	NP_001343.2:p.Pro239=
XM_017026388.2:c.287C=	XP_016881877.1:p.Pro96=
XR_243907.4:n.1621C=
NM_001352.5:c.716C= MANE Select	NP_001343.2:p.Pro239=