Canonical Allele Identifier: CA1877196431

Gene: DAB2IP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121713952_121713953delinsCA , CM000671.2:g.121713952_121713953delinsCA	GRCh38
NC_000009.11:g.124476231_124476232delinsCA , CM000671.1:g.124476231_124476232delinsCA	GRCh37
NC_000009.10:g.123516052_123516053delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408936.8:c.362+14494_362+14495delinsCA MANE Select	ENSP00000386183.3:n.362+14494_362+14495delinsCA
ENST00000699487.1:c.218+12839_218+12840delinsCA	ENSP00000514398.1:n.218+12839_218+12840delinsCA
ENST00000259371.7:c.278+14494_278+14495delinsCA	ENSP00000259371.2:n.278+14494_278+14495delinsCA
ENST00000436835.6:c.144+35171_144+35172delinsCA	ENSP00000409327.2:n.144+35171_144+35172delinsCA
ENST00000259371.6:c.278+14494_278+14495delinsCA	ENSP00000259371.2:n.278+14494_278+14495delinsCA
ENST00000373782.7:c.89+14494_89+14495delinsCA	ENSP00000362887.3:n.89+14494_89+14495delinsCA
ENST00000394340.7:c.278+14494_278+14495delinsCA	ENSP00000377872.3:n.278+14494_278+14495delinsCA
ENST00000408936.7:c.362+14494_362+14495delinsCA	ENSP00000386183.3:n.362+14494_362+14495delinsCA
ENST00000436835.5:c.-11+35171_-11+35172delinsCA	ENSP00000409327.1:n.-11+35171_-11+35172delinsCA
NM_032552.3:c.278+14494_278+14495delinsCA	NP_115941.2:n.278+14494_278+14495delinsCA
XM_005251719.3:c.362+14494_362+14495delinsCA	XP_005251776.1:n.362+14494_362+14495delinsCA
XM_005251721.1:c.278+14494_278+14495delinsCA	XP_005251778.1:n.278+14494_278+14495delinsCA
XM_011518264.1:c.341+14494_341+14495delinsCA	XP_011516566.1:n.341+14494_341+14495delinsCA
XM_011518265.1:c.341+14494_341+14495delinsCA	XP_011516567.1:n.341+14494_341+14495delinsCA
XM_011518266.1:c.341+14494_341+14495delinsCA	XP_011516568.1:n.341+14494_341+14495delinsCA
XM_011518267.1:c.341+14494_341+14495delinsCA	XP_011516569.1:n.341+14494_341+14495delinsCA
XM_011518268.1:c.341+14494_341+14495delinsCA	XP_011516570.1:n.341+14494_341+14495delinsCA
XM_011518271.1:c.-11+14291_-11+14292delinsCA	XP_011516573.1:n.-11+14291_-11+14292delinsCA
XM_005251719.4:c.362+14494_362+14495delinsCA	XP_005251776.1:n.362+14494_362+14495delinsCA
XM_011518264.3:c.341+14494_341+14495delinsCA	XP_011516566.1:n.341+14494_341+14495delinsCA
XM_011518265.3:c.341+14494_341+14495delinsCA	XP_011516567.1:n.341+14494_341+14495delinsCA
XM_011518266.2:c.341+14494_341+14495delinsCA	XP_011516568.1:n.341+14494_341+14495delinsCA
XM_011518267.2:c.341+14494_341+14495delinsCA	XP_011516569.1:n.341+14494_341+14495delinsCA
XM_011518271.2:c.-11+14291_-11+14292delinsCA	XP_011516573.1:n.-11+14291_-11+14292delinsCA
XM_017014299.1:c.218+12839_218+12840delinsCA	XP_016869788.1:n.218+12839_218+12840delinsCA
XM_017014300.1:c.-11+14494_-11+14495delinsCA	XP_016869789.1:n.-11+14494_-11+14495delinsCA
XM_024447418.1:c.170+14494_170+14495delinsCA	XP_024303186.1:n.170+14494_170+14495delinsCA
NM_032552.4:c.278+14494_278+14495delinsCA	NP_115941.2:n.278+14494_278+14495delinsCA
NM_001395010.1:c.362+14494_362+14495delinsCA MANE Select	NP_001381939.1:n.362+14494_362+14495delinsCA