Canonical Allele Identifier: CA2577833665
Gene: DCBLD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881459_98881462del , CM000665.2:g.98881459_98881462del GRCh38
NC_000003.11:g.98600303_98600306del , CM000665.1:g.98600303_98600306del GRCh37
NC_000003.10:g.100082993_100082996del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326840.11:c.433+78_433+81del MANE Select ENSP00000321573.6:n.433+78_433+81del
ENST00000326840.10:c.433+78_433+81del ENSP00000321573.6:n.433+78_433+81del
ENST00000326857.9:c.433+78_433+81del ENSP00000321646.9:n.433+78_433+81del
ENST00000449482.1:c.115+78_115+81del ENSP00000396803.1:n.115+78_115+81del
ENST00000469648.5:n.268+19260_268+19263del
ENST00000486004.1:n.411+78_411+81del
NM_080927.3:c.433+78_433+81del NP_563615.3:n.433+78_433+81del
XM_011512419.1:c.205+19660_205+19663del XP_011510721.1:n.205+19660_205+19663del
XM_011512419.2:c.205+19660_205+19663del XP_011510721.1:n.205+19660_205+19663del
XM_024453347.1:c.115+78_115+81del XP_024309115.1:n.115+78_115+81del
XM_024453348.1:c.115+78_115+81del XP_024309116.1:n.115+78_115+81del
NM_080927.4:c.433+78_433+81del MANE Select NP_563615.3:n.433+78_433+81del