Canonical Allele Identifier: CA1128857023

Gene: DAB2IP

Linked Data

• dbSNP Id: rs1833363185
• gnomAD v3: 9-121665070-G-A
• gnomAD v4: 9-121665070-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121665070G>A , CM000671.2:g.121665070G>A	GRCh38
NC_000009.11:g.124427349G>A , CM000671.1:g.124427349G>A	GRCh37
NC_000009.10:g.123467170G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000408936.8:c.124+13171G>A MANE Select	ENSP00000386183.3:n.124+13171G>A
ENST00000259371.7:c.41-13608G>A	ENSP00000259371.2:n.41-13608G>A
ENST00000436835.6:c.41-13608G>A	ENSP00000409327.2:n.41-13608G>A
ENST00000259371.6:c.41-13608G>A	ENSP00000259371.2:n.41-13608G>A
ENST00000394340.7:c.41-13608G>A	ENSP00000377872.3:n.41-13608G>A
ENST00000408936.7:c.124+13171G>A	ENSP00000386183.3:n.124+13171G>A
ENST00000436835.5:c.-114-13608G>A	ENSP00000409327.1:n.-114-13608G>A
ENST00000465078.1:n.215+13171G>A
ENST00000489314.1:n.360-13608G>A
NM_032552.3:c.41-13608G>A	NP_115941.2:n.41-13608G>A
XM_005251719.3:c.124+13171G>A	XP_005251776.1:n.124+13171G>A
XM_005251721.1:c.41-13608G>A	XP_005251778.1:n.41-13608G>A
XM_011518264.1:c.104-13608G>A	XP_011516566.1:n.104-13608G>A
XM_011518265.1:c.104-13608G>A	XP_011516567.1:n.104-13608G>A
XM_011518266.1:c.104-13608G>A	XP_011516568.1:n.104-13608G>A
XM_011518267.1:c.104-13608G>A	XP_011516569.1:n.104-13608G>A
XM_011518268.1:c.104-13608G>A	XP_011516570.1:n.104-13608G>A
XM_005251719.4:c.124+13171G>A	XP_005251776.1:n.124+13171G>A
XM_011518264.3:c.104-13608G>A	XP_011516566.1:n.104-13608G>A
XM_011518265.3:c.104-13608G>A	XP_011516567.1:n.104-13608G>A
XM_011518266.2:c.104-13608G>A	XP_011516568.1:n.104-13608G>A
XM_011518267.2:c.104-13608G>A	XP_011516569.1:n.104-13608G>A
XM_024447418.1:c.-68-13608G>A	XP_024303186.1:n.-68-13608G>A
NM_032552.4:c.41-13608G>A	NP_115941.2:n.41-13608G>A
NM_001395010.1:c.124+13171G>A MANE Select	NP_001381939.1:n.124+13171G>A