Canonical Allele Identifier: CA1931534899

Gene: DNMBP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99912647G= , CM000672.2:g.99912647G=	GRCh38
NC_000010.10:g.101672404G= , CM000672.1:g.101672404G=	GRCh37
NC_000010.9:g.101662394G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324109.9:c.2261-3501C= MANE Select	ENSP00000315659.4:n.2261-3501C=
ENST00000543621.6:c.124+1306C=	ENSP00000443657.2:n.124+1306C=
ENST00000636706.1:c.1157-3501C=	ENSP00000489875.1:n.1157-3501C=
ENST00000324109.8:c.2261-3501C=	ENSP00000315659.4:n.2261-3501C=
ENST00000422692.1:c.124+1306C=	ENSP00000409476.1:n.124+1306C=
ENST00000543621.5:c.-3+1306C=	ENSP00000443657.1:n.-3+1306C=
NM_015221.2:c.2261-3501C=	NP_056036.1:n.2261-3501C=
XM_006717735.2:c.2261-3501C=	XP_006717798.1:n.2261-3501C=
XM_006717736.2:c.2261-3501C=	XP_006717799.1:n.2261-3501C=
XM_011539559.1:c.2261-3501C=	XP_011537861.1:n.2261-3501C=
XM_011539560.1:c.1157-3501C=	XP_011537862.1:n.1157-3501C=
NM_001318326.1:c.1157-3501C=	NP_001305255.1:n.1157-3501C=
NM_001318327.1:c.124+1306C=	NP_001305256.1:n.124+1306C=
NM_015221.3:c.2261-3501C=	NP_056036.1:n.2261-3501C=
XM_006717735.3:c.2261-3501C=	XP_006717798.1:n.2261-3501C=
XM_011539559.2:c.2261-3501C=	XP_011537861.1:n.2261-3501C=
NM_015221.4:c.2261-3501C= MANE Select	NP_056036.1:n.2261-3501C=
NM_001318326.2:c.1157-3501C=	NP_001305255.1:n.1157-3501C=