Canonical Allele Identifier: CA1168873516
Gene: DAB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.57160217T= , CM000663.2:g.57160217T= GRCh38
NC_000001.10:g.57625890T= , CM000663.1:g.57625890T= GRCh37
NC_000001.9:g.57398478T= NCBI36
NG_046914.2:g.1095331A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371236.7:c.68-14788A= MANE Select ENSP00000360280.1:n.68-14788A=
ENST00000332102.10:c.68-14788A= ENSP00000329120.6:n.68-14788A=
ENST00000371230.1:c.68-14788A= ENSP00000360274.1:n.68-14788A=
ENST00000371231.5:c.68-14788A= ENSP00000360275.1:n.68-14788A=
ENST00000371232.8:c.68-14788A= ENSP00000360276.4:n.68-14788A=
ENST00000371236.6:c.68-14788A= ENSP00000360280.1:n.68-14788A=
ENST00000414851.6:c.68-14788A= ENSP00000387581.3:n.68-14788A=
ENST00000420954.6:c.68-14788A= ENSP00000395296.2:n.68-14788A=
ENST00000473821.1:n.710-14788A=
ENST00000485760.5:n.829-14788A=
NM_021080.3:c.68-14788A= NP_066566.3:n.68-14788A=
NM_001353980.1:c.68-14788A= NP_001340909.1:n.68-14788A=
NM_001353983.1:c.68-14788A= NP_001340912.1:n.68-14788A=
NM_001353985.1:c.68-14788A= NP_001340914.1:n.68-14788A=
NM_001353986.1:c.68-14788A= NP_001340915.1:n.68-14788A=
NM_001365792.1:c.68-14788A= MANE Select NP_001352721.1:n.68-14788A=
NM_001365793.1:c.68-14788A= NP_001352722.1:n.68-14788A=
NM_001365794.1:c.68-14788A= NP_001352723.1:n.68-14788A=
NM_001365795.1:c.68-14788A= NP_001352724.1:n.68-14788A=
NM_001365796.1:c.68-14788A= NP_001352725.1:n.68-14788A=
NM_021080.4:c.68-14788A= NP_066566.3:n.68-14788A=
NM_001353985.2:c.68-14788A= NP_001340914.1:n.68-14788A=
NM_001353986.2:c.68-14788A= NP_001340915.1:n.68-14788A=
NM_021080.5:c.68-14788A= NP_066566.3:n.68-14788A=
NM_001353980.2:c.68-14788A= NP_001340909.1:n.68-14788A=
NM_001353983.2:c.68-14788A= NP_001340912.1:n.68-14788A=
NM_001365794.2:c.68-14788A= NP_001352723.1:n.68-14788A=
NM_001365795.2:c.68-14788A= NP_001352724.1:n.68-14788A=
NM_001379461.1:c.68-14788A= NP_001366390.1:n.68-14788A=
NM_001379462.1:c.68-14788A= NP_001366391.1:n.68-14788A=