Canonical Allele Identifier: CA1931534888

Gene: DNMBP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99912633_99912645delinsTGGGTGGGACCGG , CM000672.2:g.99912633_99912645delinsTGGGTGGGACCGG	GRCh38
NC_000010.10:g.101672390_101672402delinsTGGGTGGGACCGG , CM000672.1:g.101672390_101672402delinsTGGGTGGGACCGG	GRCh37
NC_000010.9:g.101662380_101662392delinsTGGGTGGGACCGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324109.9:c.2261-3499_2261-3487delinsCCGGTCCCACCCA MANE Select	ENSP00000315659.4:n.2261-3499_2261-3487de...
ENST00000543621.6:c.124+1308_124+1320delinsCCGGTCCCACCCA	ENSP00000443657.2:n.124+1308_124+1320deli...
ENST00000636706.1:c.1157-3499_1157-3487delinsCCGGTCCCACCCA	ENSP00000489875.1:n.1157-3499_1157-3487de...
ENST00000324109.8:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	ENSP00000315659.4:n.2261-3499_2261-3487de...
ENST00000422692.1:c.124+1308_124+1320delinsCCGGTCCCACCCA	ENSP00000409476.1:n.124+1308_124+1320deli...
ENST00000543621.5:c.-3+1308_-3+1320delinsCCGGTCCCACCCA	ENSP00000443657.1:n.-3+1308_-3+1320delins...
NM_015221.2:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	NP_056036.1:n.2261-3499_2261-3487delinsCC...
XM_006717735.2:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	XP_006717798.1:n.2261-3499_2261-3487delin...
XM_006717736.2:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	XP_006717799.1:n.2261-3499_2261-3487delin...
XM_011539559.1:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	XP_011537861.1:n.2261-3499_2261-3487delin...
XM_011539560.1:c.1157-3499_1157-3487delinsCCGGTCCCACCCA	XP_011537862.1:n.1157-3499_1157-3487delin...
NM_001318326.1:c.1157-3499_1157-3487delinsCCGGTCCCACCCA	NP_001305255.1:n.1157-3499_1157-3487delin...
NM_001318327.1:c.124+1308_124+1320delinsCCGGTCCCACCCA	NP_001305256.1:n.124+1308_124+1320delinsC...
NM_015221.3:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	NP_056036.1:n.2261-3499_2261-3487delinsCC...
XM_006717735.3:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	XP_006717798.1:n.2261-3499_2261-3487delin...
XM_011539559.2:c.2261-3499_2261-3487delinsCCGGTCCCACCCA	XP_011537861.1:n.2261-3499_2261-3487delin...
NM_015221.4:c.2261-3499_2261-3487delinsCCGGTCCCACCCA MANE Select	NP_056036.1:n.2261-3499_2261-3487delinsCC...
NM_001318326.2:c.1157-3499_1157-3487delinsCCGGTCCCACCCA	NP_001305255.1:n.1157-3499_1157-3487delin...