Canonical Allele Identifier: CA1128844096

Gene: DAB2IP

Linked Data

• dbSNP Id: rs1830435599
• gnomAD v3: 9-121713486-ACT-A
• gnomAD v4: 9-121713486-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121713490_121713491del , CM000671.2:g.121713490_121713491del	GRCh38
NC_000009.11:g.124475769_124475770del , CM000671.1:g.124475769_124475770del	GRCh37
NC_000009.10:g.123515590_123515591del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408936.8:c.362+14032_362+14033del MANE Select	ENSP00000386183.3:n.362+14032_362+14033del
ENST00000699487.1:c.218+12377_218+12378del	ENSP00000514398.1:n.218+12377_218+12378del
ENST00000259371.7:c.278+14032_278+14033del	ENSP00000259371.2:n.278+14032_278+14033del
ENST00000436835.6:c.144+34709_144+34710del	ENSP00000409327.2:n.144+34709_144+34710del
ENST00000259371.6:c.278+14032_278+14033del	ENSP00000259371.2:n.278+14032_278+14033del
ENST00000373782.7:c.89+14032_89+14033del	ENSP00000362887.3:n.89+14032_89+14033del
ENST00000394340.7:c.278+14032_278+14033del	ENSP00000377872.3:n.278+14032_278+14033del
ENST00000408936.7:c.362+14032_362+14033del	ENSP00000386183.3:n.362+14032_362+14033del
ENST00000436835.5:c.-11+34709_-11+34710del	ENSP00000409327.1:n.-11+34709_-11+34710del
NM_032552.3:c.278+14032_278+14033del	NP_115941.2:n.278+14032_278+14033del
XM_005251719.3:c.362+14032_362+14033del	XP_005251776.1:n.362+14032_362+14033del
XM_005251721.1:c.278+14032_278+14033del	XP_005251778.1:n.278+14032_278+14033del
XM_011518264.1:c.341+14032_341+14033del	XP_011516566.1:n.341+14032_341+14033del
XM_011518265.1:c.341+14032_341+14033del	XP_011516567.1:n.341+14032_341+14033del
XM_011518266.1:c.341+14032_341+14033del	XP_011516568.1:n.341+14032_341+14033del
XM_011518267.1:c.341+14032_341+14033del	XP_011516569.1:n.341+14032_341+14033del
XM_011518268.1:c.341+14032_341+14033del	XP_011516570.1:n.341+14032_341+14033del
XM_011518271.1:c.-11+13829_-11+13830del	XP_011516573.1:n.-11+13829_-11+13830del
XM_005251719.4:c.362+14032_362+14033del	XP_005251776.1:n.362+14032_362+14033del
XM_011518264.3:c.341+14032_341+14033del	XP_011516566.1:n.341+14032_341+14033del
XM_011518265.3:c.341+14032_341+14033del	XP_011516567.1:n.341+14032_341+14033del
XM_011518266.2:c.341+14032_341+14033del	XP_011516568.1:n.341+14032_341+14033del
XM_011518267.2:c.341+14032_341+14033del	XP_011516569.1:n.341+14032_341+14033del
XM_011518271.2:c.-11+13829_-11+13830del	XP_011516573.1:n.-11+13829_-11+13830del
XM_017014299.1:c.218+12377_218+12378del	XP_016869788.1:n.218+12377_218+12378del
XM_017014300.1:c.-11+14032_-11+14033del	XP_016869789.1:n.-11+14032_-11+14033del
XM_024447418.1:c.170+14032_170+14033del	XP_024303186.1:n.170+14032_170+14033del
NM_032552.4:c.278+14032_278+14033del	NP_115941.2:n.278+14032_278+14033del
NM_001395010.1:c.362+14032_362+14033del MANE Select	NP_001381939.1:n.362+14032_362+14033del