Canonical Allele Identifier: CA1877160022

Gene: DAB2IP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121634063_121634064delinsCT , CM000671.2:g.121634063_121634064delinsCT	GRCh38
NC_000009.11:g.124396342_124396343delinsCT , CM000671.1:g.124396342_124396343delinsCT	GRCh37
NC_000009.10:g.123436163_123436164delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259371.7:c.41-44615_41-44614delinsCT	ENSP00000259371.2:n.41-44615_41-44614delinsCT
ENST00000436835.6:c.41-44615_41-44614delinsCT	ENSP00000409327.2:n.41-44615_41-44614delinsCT
ENST00000259371.6:c.41-44615_41-44614delinsCT	ENSP00000259371.2:n.41-44615_41-44614delinsCT
ENST00000394340.7:c.41-44615_41-44614delinsCT	ENSP00000377872.3:n.41-44615_41-44614delinsCT
ENST00000436835.5:c.-114-44615_-114-44614delinsCT	ENSP00000409327.1:n.-114-44615_-114-44614delinsCT
ENST00000489314.1:n.359+35437_359+35438delinsCT
NM_032552.3:c.41-44615_41-44614delinsCT	NP_115941.2:n.41-44615_41-44614delinsCT
XM_005251721.1:c.41-44615_41-44614delinsCT	XP_005251778.1:n.41-44615_41-44614delinsCT
XM_011518264.1:c.103+35437_103+35438delinsCT	XP_011516566.1:n.103+35437_103+35438delinsCT
XM_011518265.1:c.103+35437_103+35438delinsCT	XP_011516567.1:n.103+35437_103+35438delinsCT
XM_011518266.1:c.103+35437_103+35438delinsCT	XP_011516568.1:n.103+35437_103+35438delinsCT
XM_011518267.1:c.103+35437_103+35438delinsCT	XP_011516569.1:n.103+35437_103+35438delinsCT
XM_011518268.1:c.103+35437_103+35438delinsCT	XP_011516570.1:n.103+35437_103+35438delinsCT
XM_011518264.3:c.103+35437_103+35438delinsCT	XP_011516566.1:n.103+35437_103+35438delinsCT
XM_011518265.3:c.103+35437_103+35438delinsCT	XP_011516567.1:n.103+35437_103+35438delinsCT
XM_011518266.2:c.103+35437_103+35438delinsCT	XP_011516568.1:n.103+35437_103+35438delinsCT
XM_011518267.2:c.103+35437_103+35438delinsCT	XP_011516569.1:n.103+35437_103+35438delinsCT
XM_024447418.1:c.-69+34297_-69+34298delinsCT	XP_024303186.1:n.-69+34297_-69+34298delinsCT
NM_032552.4:c.41-44615_41-44614delinsCT	NP_115941.2:n.41-44615_41-44614delinsCT