Canonical Allele Identifier: CA1877196206

Gene: DAB2IP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121713514_121713517delinsCTTG , CM000671.2:g.121713514_121713517delinsCTTG	GRCh38
NC_000009.11:g.124475793_124475796delinsCTTG , CM000671.1:g.124475793_124475796delinsCTTG	GRCh37
NC_000009.10:g.123515614_123515617delinsCTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408936.8:c.362+14056_362+14059delinsCTTG MANE Select	ENSP00000386183.3:n.362+14056_362+14059delinsCTTG
ENST00000699487.1:c.218+12401_218+12404delinsCTTG	ENSP00000514398.1:n.218+12401_218+12404delinsCTTG
ENST00000259371.7:c.278+14056_278+14059delinsCTTG	ENSP00000259371.2:n.278+14056_278+14059delinsCTTG
ENST00000436835.6:c.144+34733_144+34736delinsCTTG	ENSP00000409327.2:n.144+34733_144+34736delinsCTTG
ENST00000259371.6:c.278+14056_278+14059delinsCTTG	ENSP00000259371.2:n.278+14056_278+14059delinsCTTG
ENST00000373782.7:c.89+14056_89+14059delinsCTTG	ENSP00000362887.3:n.89+14056_89+14059delinsCTTG
ENST00000394340.7:c.278+14056_278+14059delinsCTTG	ENSP00000377872.3:n.278+14056_278+14059delinsCTTG
ENST00000408936.7:c.362+14056_362+14059delinsCTTG	ENSP00000386183.3:n.362+14056_362+14059delinsCTTG
ENST00000436835.5:c.-11+34733_-11+34736delinsCTTG	ENSP00000409327.1:n.-11+34733_-11+34736delinsCTTG
NM_032552.3:c.278+14056_278+14059delinsCTTG	NP_115941.2:n.278+14056_278+14059delinsCTTG
XM_005251719.3:c.362+14056_362+14059delinsCTTG	XP_005251776.1:n.362+14056_362+14059delinsCTTG
XM_005251721.1:c.278+14056_278+14059delinsCTTG	XP_005251778.1:n.278+14056_278+14059delinsCTTG
XM_011518264.1:c.341+14056_341+14059delinsCTTG	XP_011516566.1:n.341+14056_341+14059delinsCTTG
XM_011518265.1:c.341+14056_341+14059delinsCTTG	XP_011516567.1:n.341+14056_341+14059delinsCTTG
XM_011518266.1:c.341+14056_341+14059delinsCTTG	XP_011516568.1:n.341+14056_341+14059delinsCTTG
XM_011518267.1:c.341+14056_341+14059delinsCTTG	XP_011516569.1:n.341+14056_341+14059delinsCTTG
XM_011518268.1:c.341+14056_341+14059delinsCTTG	XP_011516570.1:n.341+14056_341+14059delinsCTTG
XM_011518271.1:c.-11+13853_-11+13856delinsCTTG	XP_011516573.1:n.-11+13853_-11+13856delinsCTTG
XM_005251719.4:c.362+14056_362+14059delinsCTTG	XP_005251776.1:n.362+14056_362+14059delinsCTTG
XM_011518264.3:c.341+14056_341+14059delinsCTTG	XP_011516566.1:n.341+14056_341+14059delinsCTTG
XM_011518265.3:c.341+14056_341+14059delinsCTTG	XP_011516567.1:n.341+14056_341+14059delinsCTTG
XM_011518266.2:c.341+14056_341+14059delinsCTTG	XP_011516568.1:n.341+14056_341+14059delinsCTTG
XM_011518267.2:c.341+14056_341+14059delinsCTTG	XP_011516569.1:n.341+14056_341+14059delinsCTTG
XM_011518271.2:c.-11+13853_-11+13856delinsCTTG	XP_011516573.1:n.-11+13853_-11+13856delinsCTTG
XM_017014299.1:c.218+12401_218+12404delinsCTTG	XP_016869788.1:n.218+12401_218+12404delinsCTTG
XM_017014300.1:c.-11+14056_-11+14059delinsCTTG	XP_016869789.1:n.-11+14056_-11+14059delinsCTTG
XM_024447418.1:c.170+14056_170+14059delinsCTTG	XP_024303186.1:n.170+14056_170+14059delinsCTTG
NM_032552.4:c.278+14056_278+14059delinsCTTG	NP_115941.2:n.278+14056_278+14059delinsCTTG
NM_001395010.1:c.362+14056_362+14059delinsCTTG MANE Select	NP_001381939.1:n.362+14056_362+14059delinsCTTG