Canonical Allele Identifier: CA670662616

Gene: DNMBP

Linked Data

• dbSNP Id: rs1383650546
• gnomAD v3: 10-99912440-AAAAC-A
• gnomAD v4: 10-99912440-AAAAC-A
• MyVariant Identifiers: chr10:g.101672198_101672201del (hg19) ; chr10:g.99912441_99912444del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99912443_99912446del , CM000672.2:g.99912443_99912446del	GRCh38
NC_000010.10:g.101672200_101672203del , CM000672.1:g.101672200_101672203del	GRCh37
NC_000010.9:g.101662190_101662193del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324109.9:c.2261-3298_2261-3295del MANE Select	ENSP00000315659.4:n.2261-3298_2261-3295del
ENST00000543621.6:c.124+1509_124+1512del	ENSP00000443657.2:n.124+1509_124+1512del
ENST00000636706.1:c.1157-3298_1157-3295del	ENSP00000489875.1:n.1157-3298_1157-3295del
ENST00000324109.8:c.2261-3298_2261-3295del	ENSP00000315659.4:n.2261-3298_2261-3295del
ENST00000422692.1:c.124+1509_124+1512del	ENSP00000409476.1:n.124+1509_124+1512del
ENST00000543621.5:c.-3+1509_-3+1512del	ENSP00000443657.1:n.-3+1509_-3+1512del
NM_015221.2:c.2261-3298_2261-3295del	NP_056036.1:n.2261-3298_2261-3295del
XM_006717735.2:c.2261-3298_2261-3295del	XP_006717798.1:n.2261-3298_2261-3295del
XM_006717736.2:c.2261-3298_2261-3295del	XP_006717799.1:n.2261-3298_2261-3295del
XM_011539559.1:c.2261-3298_2261-3295del	XP_011537861.1:n.2261-3298_2261-3295del
XM_011539560.1:c.1157-3298_1157-3295del	XP_011537862.1:n.1157-3298_1157-3295del
NM_001318326.1:c.1157-3298_1157-3295del	NP_001305255.1:n.1157-3298_1157-3295del
NM_001318327.1:c.124+1509_124+1512del	NP_001305256.1:n.124+1509_124+1512del
NM_015221.3:c.2261-3298_2261-3295del	NP_056036.1:n.2261-3298_2261-3295del
XM_006717735.3:c.2261-3298_2261-3295del	XP_006717798.1:n.2261-3298_2261-3295del
XM_011539559.2:c.2261-3298_2261-3295del	XP_011537861.1:n.2261-3298_2261-3295del
NM_015221.4:c.2261-3298_2261-3295del MANE Select	NP_056036.1:n.2261-3298_2261-3295del
NM_001318326.2:c.1157-3298_1157-3295del	NP_001305255.1:n.1157-3298_1157-3295del