Canonical Allele Identifier: CA1877181249
Gene: DAB2IP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121660200C= , CM000671.2:g.121660200C= GRCh38
NC_000009.11:g.124422479C= , CM000671.1:g.124422479C= GRCh37
NC_000009.10:g.123462300C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000408936.8:c.124+8301C= MANE Select ENSP00000386183.3:n.124+8301C=
ENST00000259371.7:c.41-18478C= ENSP00000259371.2:n.41-18478C=
ENST00000436835.6:c.41-18478C= ENSP00000409327.2:n.41-18478C=
ENST00000259371.6:c.41-18478C= ENSP00000259371.2:n.41-18478C=
ENST00000394340.7:c.41-18478C= ENSP00000377872.3:n.41-18478C=
ENST00000408936.7:c.124+8301C= ENSP00000386183.3:n.124+8301C=
ENST00000436835.5:c.-114-18478C= ENSP00000409327.1:n.-114-18478C=
ENST00000465078.1:n.215+8301C=
ENST00000489314.1:n.360-18478C=
NM_032552.3:c.41-18478C= NP_115941.2:n.41-18478C=
XM_005251719.3:c.124+8301C= XP_005251776.1:n.124+8301C=
XM_005251721.1:c.41-18478C= XP_005251778.1:n.41-18478C=
XM_011518264.1:c.104-18478C= XP_011516566.1:n.104-18478C=
XM_011518265.1:c.104-18478C= XP_011516567.1:n.104-18478C=
XM_011518266.1:c.104-18478C= XP_011516568.1:n.104-18478C=
XM_011518267.1:c.104-18478C= XP_011516569.1:n.104-18478C=
XM_011518268.1:c.104-18478C= XP_011516570.1:n.104-18478C=
XM_005251719.4:c.124+8301C= XP_005251776.1:n.124+8301C=
XM_011518264.3:c.104-18478C= XP_011516566.1:n.104-18478C=
XM_011518265.3:c.104-18478C= XP_011516567.1:n.104-18478C=
XM_011518266.2:c.104-18478C= XP_011516568.1:n.104-18478C=
XM_011518267.2:c.104-18478C= XP_011516569.1:n.104-18478C=
XM_024447418.1:c.-68-18478C= XP_024303186.1:n.-68-18478C=
NM_032552.4:c.41-18478C= NP_115941.2:n.41-18478C=
NM_001395010.1:c.124+8301C= MANE Select NP_001381939.1:n.124+8301C=