Canonical Allele Identifier: CA2666720434
Gene: DCBLD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881484_98881509del , CM000665.2:g.98881484_98881509del GRCh38
NC_000003.11:g.98600328_98600353del , CM000665.1:g.98600328_98600353del GRCh37
NC_000003.10:g.100083018_100083043del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326840.11:c.433+31_433+56del MANE Select ENSP00000321573.6:n.433+31_433+56del
ENST00000326840.10:c.433+31_433+56del ENSP00000321573.6:n.433+31_433+56del
ENST00000326857.9:c.433+31_433+56del ENSP00000321646.9:n.433+31_433+56del
ENST00000449482.1:c.115+31_115+56del ENSP00000396803.1:n.115+31_115+56del
ENST00000469648.5:n.268+19213_268+19238del
ENST00000486004.1:n.411+31_411+56del
NM_080927.3:c.433+31_433+56del NP_563615.3:n.433+31_433+56del
XM_011512419.1:c.205+19613_205+19638del XP_011510721.1:n.205+19613_205+19638del
XM_011512419.2:c.205+19613_205+19638del XP_011510721.1:n.205+19613_205+19638del
XM_024453347.1:c.115+31_115+56del XP_024309115.1:n.115+31_115+56del
XM_024453348.1:c.115+31_115+56del XP_024309116.1:n.115+31_115+56del
NM_080927.4:c.433+31_433+56del MANE Select NP_563615.3:n.433+31_433+56del