Canonical Allele Identifier: CA2525912959
Gene: DCBLD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881368_98881371del , CM000665.2:g.98881368_98881371del GRCh38
NC_000003.11:g.98600212_98600215del , CM000665.1:g.98600212_98600215del GRCh37
NC_000003.10:g.100082902_100082905del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326840.11:c.433+170_433+173del MANE Select ENSP00000321573.6:n.433+170_433+173del
ENST00000326840.10:c.433+170_433+173del ENSP00000321573.6:n.433+170_433+173del
ENST00000326857.9:c.433+170_433+173del ENSP00000321646.9:n.433+170_433+173del
ENST00000449482.1:c.115+170_115+173del ENSP00000396803.1:n.115+170_115+173del
ENST00000469648.5:n.268+19352_268+19355del
ENST00000486004.1:n.411+170_411+173del
NM_080927.3:c.433+170_433+173del NP_563615.3:n.433+170_433+173del
XM_011512419.1:c.205+19752_205+19755del XP_011510721.1:n.205+19752_205+19755del
XM_011512419.2:c.205+19752_205+19755del XP_011510721.1:n.205+19752_205+19755del
XM_024453347.1:c.115+170_115+173del XP_024309115.1:n.115+170_115+173del
XM_024453348.1:c.115+170_115+173del XP_024309116.1:n.115+170_115+173del
NM_080927.4:c.433+170_433+173del MANE Select NP_563615.3:n.433+170_433+173del