Canonical Allele Identifier: CA1387545089

Gene: DCBLD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98881391_98881392delinsCA , CM000665.2:g.98881391_98881392delinsCA	GRCh38
NC_000003.11:g.98600235_98600236delinsCA , CM000665.1:g.98600235_98600236delinsCA	GRCh37
NC_000003.10:g.100082925_100082926delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326840.11:c.433+148_433+149delinsTG MANE Select	ENSP00000321573.6:n.433+148_433+149delinsTG
ENST00000326840.10:c.433+148_433+149delinsTG	ENSP00000321573.6:n.433+148_433+149delinsTG
ENST00000326857.9:c.433+148_433+149delinsTG	ENSP00000321646.9:n.433+148_433+149delinsTG
ENST00000449482.1:c.115+148_115+149delinsTG	ENSP00000396803.1:n.115+148_115+149delinsTG
ENST00000469648.5:n.268+19330_268+19331delinsTG
ENST00000486004.1:n.411+148_411+149delinsTG
NM_080927.3:c.433+148_433+149delinsTG	NP_563615.3:n.433+148_433+149delinsTG
XM_011512419.1:c.205+19730_205+19731delinsTG	XP_011510721.1:n.205+19730_205+19731delinsTG
XM_011512419.2:c.205+19730_205+19731delinsTG	XP_011510721.1:n.205+19730_205+19731delinsTG
XM_024453347.1:c.115+148_115+149delinsTG	XP_024309115.1:n.115+148_115+149delinsTG
XM_024453348.1:c.115+148_115+149delinsTG	XP_024309116.1:n.115+148_115+149delinsTG
NM_080927.4:c.433+148_433+149delinsTG MANE Select	NP_563615.3:n.433+148_433+149delinsTG