Canonical Allele Identifier: CA200088483

Gene: DAB2IP

Linked Data

• dbSNP Id: rs947795668
• gnomAD v3: 9-121713441-CAG-C
• gnomAD v4: 9-121713441-CAG-C
• MyVariant Identifiers: chr9:g.124475721_124475722del (hg19) ; chr9:g.121713442_121713443del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121713442_121713443del , CM000671.2:g.121713442_121713443del	GRCh38
NC_000009.11:g.124475721_124475722del , CM000671.1:g.124475721_124475722del	GRCh37
NC_000009.10:g.123515542_123515543del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408936.8:c.362+13984_362+13985del MANE Select	ENSP00000386183.3:n.362+13984_362+13985del
ENST00000699487.1:c.218+12329_218+12330del	ENSP00000514398.1:n.218+12329_218+12330del
ENST00000259371.7:c.278+13984_278+13985del	ENSP00000259371.2:n.278+13984_278+13985del
ENST00000436835.6:c.144+34661_144+34662del	ENSP00000409327.2:n.144+34661_144+34662del
ENST00000259371.6:c.278+13984_278+13985del	ENSP00000259371.2:n.278+13984_278+13985del
ENST00000373782.7:c.89+13984_89+13985del	ENSP00000362887.3:n.89+13984_89+13985del
ENST00000394340.7:c.278+13984_278+13985del	ENSP00000377872.3:n.278+13984_278+13985del
ENST00000408936.7:c.362+13984_362+13985del	ENSP00000386183.3:n.362+13984_362+13985del
ENST00000436835.5:c.-11+34661_-11+34662del	ENSP00000409327.1:n.-11+34661_-11+34662del
NM_032552.3:c.278+13984_278+13985del	NP_115941.2:n.278+13984_278+13985del
XM_005251719.3:c.362+13984_362+13985del	XP_005251776.1:n.362+13984_362+13985del
XM_005251721.1:c.278+13984_278+13985del	XP_005251778.1:n.278+13984_278+13985del
XM_011518264.1:c.341+13984_341+13985del	XP_011516566.1:n.341+13984_341+13985del
XM_011518265.1:c.341+13984_341+13985del	XP_011516567.1:n.341+13984_341+13985del
XM_011518266.1:c.341+13984_341+13985del	XP_011516568.1:n.341+13984_341+13985del
XM_011518267.1:c.341+13984_341+13985del	XP_011516569.1:n.341+13984_341+13985del
XM_011518268.1:c.341+13984_341+13985del	XP_011516570.1:n.341+13984_341+13985del
XM_011518271.1:c.-11+13781_-11+13782del	XP_011516573.1:n.-11+13781_-11+13782del
XM_005251719.4:c.362+13984_362+13985del	XP_005251776.1:n.362+13984_362+13985del
XM_011518264.3:c.341+13984_341+13985del	XP_011516566.1:n.341+13984_341+13985del
XM_011518265.3:c.341+13984_341+13985del	XP_011516567.1:n.341+13984_341+13985del
XM_011518266.2:c.341+13984_341+13985del	XP_011516568.1:n.341+13984_341+13985del
XM_011518267.2:c.341+13984_341+13985del	XP_011516569.1:n.341+13984_341+13985del
XM_011518271.2:c.-11+13781_-11+13782del	XP_011516573.1:n.-11+13781_-11+13782del
XM_017014299.1:c.218+12329_218+12330del	XP_016869788.1:n.218+12329_218+12330del
XM_017014300.1:c.-11+13984_-11+13985del	XP_016869789.1:n.-11+13984_-11+13985del
XM_024447418.1:c.170+13984_170+13985del	XP_024303186.1:n.170+13984_170+13985del
NM_032552.4:c.278+13984_278+13985del	NP_115941.2:n.278+13984_278+13985del
NM_001395010.1:c.362+13984_362+13985del MANE Select	NP_001381939.1:n.362+13984_362+13985del