Canonical Allele Identifier: CA1877196183

Gene: DAB2IP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121713486_121713488delinsACT , CM000671.2:g.121713486_121713488delinsACT	GRCh38
NC_000009.11:g.124475765_124475767delinsACT , CM000671.1:g.124475765_124475767delinsACT	GRCh37
NC_000009.10:g.123515586_123515588delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408936.8:c.362+14028_362+14030delinsACT MANE Select	ENSP00000386183.3:n.362+14028_362+14030delinsACT
ENST00000699487.1:c.218+12373_218+12375delinsACT	ENSP00000514398.1:n.218+12373_218+12375delinsACT
ENST00000259371.7:c.278+14028_278+14030delinsACT	ENSP00000259371.2:n.278+14028_278+14030delinsACT
ENST00000436835.6:c.144+34705_144+34707delinsACT	ENSP00000409327.2:n.144+34705_144+34707delinsACT
ENST00000259371.6:c.278+14028_278+14030delinsACT	ENSP00000259371.2:n.278+14028_278+14030delinsACT
ENST00000373782.7:c.89+14028_89+14030delinsACT	ENSP00000362887.3:n.89+14028_89+14030delinsACT
ENST00000394340.7:c.278+14028_278+14030delinsACT	ENSP00000377872.3:n.278+14028_278+14030delinsACT
ENST00000408936.7:c.362+14028_362+14030delinsACT	ENSP00000386183.3:n.362+14028_362+14030delinsACT
ENST00000436835.5:c.-11+34705_-11+34707delinsACT	ENSP00000409327.1:n.-11+34705_-11+34707delinsACT
NM_032552.3:c.278+14028_278+14030delinsACT	NP_115941.2:n.278+14028_278+14030delinsACT
XM_005251719.3:c.362+14028_362+14030delinsACT	XP_005251776.1:n.362+14028_362+14030delinsACT
XM_005251721.1:c.278+14028_278+14030delinsACT	XP_005251778.1:n.278+14028_278+14030delinsACT
XM_011518264.1:c.341+14028_341+14030delinsACT	XP_011516566.1:n.341+14028_341+14030delinsACT
XM_011518265.1:c.341+14028_341+14030delinsACT	XP_011516567.1:n.341+14028_341+14030delinsACT
XM_011518266.1:c.341+14028_341+14030delinsACT	XP_011516568.1:n.341+14028_341+14030delinsACT
XM_011518267.1:c.341+14028_341+14030delinsACT	XP_011516569.1:n.341+14028_341+14030delinsACT
XM_011518268.1:c.341+14028_341+14030delinsACT	XP_011516570.1:n.341+14028_341+14030delinsACT
XM_011518271.1:c.-11+13825_-11+13827delinsACT	XP_011516573.1:n.-11+13825_-11+13827delinsACT
XM_005251719.4:c.362+14028_362+14030delinsACT	XP_005251776.1:n.362+14028_362+14030delinsACT
XM_011518264.3:c.341+14028_341+14030delinsACT	XP_011516566.1:n.341+14028_341+14030delinsACT
XM_011518265.3:c.341+14028_341+14030delinsACT	XP_011516567.1:n.341+14028_341+14030delinsACT
XM_011518266.2:c.341+14028_341+14030delinsACT	XP_011516568.1:n.341+14028_341+14030delinsACT
XM_011518267.2:c.341+14028_341+14030delinsACT	XP_011516569.1:n.341+14028_341+14030delinsACT
XM_011518271.2:c.-11+13825_-11+13827delinsACT	XP_011516573.1:n.-11+13825_-11+13827delinsACT
XM_017014299.1:c.218+12373_218+12375delinsACT	XP_016869788.1:n.218+12373_218+12375delinsACT
XM_017014300.1:c.-11+14028_-11+14030delinsACT	XP_016869789.1:n.-11+14028_-11+14030delinsACT
XM_024447418.1:c.170+14028_170+14030delinsACT	XP_024303186.1:n.170+14028_170+14030delinsACT
NM_032552.4:c.278+14028_278+14030delinsACT	NP_115941.2:n.278+14028_278+14030delinsACT
NM_001395010.1:c.362+14028_362+14030delinsACT MANE Select	NP_001381939.1:n.362+14028_362+14030delinsACT