Canonical Allele Identifier: CA2655037836

Gene: DIP2A

Linked Data

• gnomAD v4: 21-46550227-TTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46550235_46550237del , CM000683.2:g.46550235_46550237del	GRCh38
NC_000021.8:g.47970148_47970150del , CM000683.1:g.47970148_47970150del	GRCh37
NC_000021.7:g.46794576_46794578del	NCBI36
NG_015996.1:g.96287_96289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417564.3:c.2638-308_2638-306del MANE Select	ENSP00000392066.2:n.2638-308_2638-306del
ENST00000651436.1:c.2638-308_2638-306del	ENSP00000498874.1:n.2638-308_2638-306del
ENST00000400274.5:c.2626-308_2626-306del	ENSP00000383133.1:n.2626-308_2626-306del
ENST00000417564.2:c.2638-308_2638-306del	ENSP00000392066.2:n.2638-308_2638-306del
NM_001146116.1:c.2626-308_2626-306del	NP_001139588.1:n.2626-308_2626-306del
NM_015151.3:c.2638-308_2638-306del	NP_055966.2:n.2638-308_2638-306del
XM_011529488.1:c.2746-308_2746-306del	XP_011527790.1:n.2746-308_2746-306del
XM_011529489.1:c.2746-308_2746-306del	XP_011527791.1:n.2746-308_2746-306del
XM_011529490.1:c.2746-308_2746-306del	XP_011527792.1:n.2746-308_2746-306del
XM_011529491.1:c.2743-308_2743-306del	XP_011527793.1:n.2743-308_2743-306del
XM_011529492.1:c.2746-308_2746-306del	XP_011527794.1:n.2746-308_2746-306del
XM_011529493.1:c.2641-308_2641-306del	XP_011527795.1:n.2641-308_2641-306del
XM_011529494.1:c.2638-308_2638-306del	XP_011527796.1:n.2638-308_2638-306del
XM_011529495.1:c.2614-308_2614-306del	XP_011527797.1:n.2614-308_2614-306del
XM_011529496.1:c.2491-308_2491-306del	XP_011527798.1:n.2491-308_2491-306del
XM_011529497.1:c.2746-308_2746-306del	XP_011527799.1:n.2746-308_2746-306del
XM_011529498.1:c.2746-308_2746-306del	XP_011527800.1:n.2746-308_2746-306del
XM_011529499.1:c.2746-308_2746-306del	XP_011527801.1:n.2746-308_2746-306del
XM_011529500.1:c.2746-308_2746-306del	XP_011527802.1:n.2746-308_2746-306del
XM_011529501.1:c.2746-308_2746-306del	XP_011527803.1:n.2746-308_2746-306del
NM_001353942.1:c.2641-308_2641-306del	NP_001340871.1:n.2641-308_2641-306del
NM_001353943.1:c.2638-308_2638-306del	NP_001340872.1:n.2638-308_2638-306del
XM_011529492.2:c.2746-308_2746-306del	XP_011527794.1:n.2746-308_2746-306del
XM_017028291.1:c.2746-308_2746-306del	XP_016883780.1:n.2746-308_2746-306del
XM_017028292.1:c.2746-308_2746-306del	XP_016883781.1:n.2746-308_2746-306del
XM_017028293.1:c.2743-308_2743-306del	XP_016883782.1:n.2743-308_2743-306del
XM_017028294.2:c.2641-308_2641-306del	XP_016883783.1:n.2641-308_2641-306del
XM_017028295.2:c.2638-308_2638-306del	XP_016883784.1:n.2638-308_2638-306del
XM_017028297.1:c.2614-308_2614-306del	XP_016883786.1:n.2614-308_2614-306del
XM_017028298.2:c.2509-308_2509-306del	XP_016883787.1:n.2509-308_2509-306del
XM_017028299.1:c.2491-308_2491-306del	XP_016883788.1:n.2491-308_2491-306del
XM_017028300.1:c.2746-308_2746-306del	XP_016883789.1:n.2746-308_2746-306del
XM_017028301.1:c.2746-308_2746-306del	XP_016883790.1:n.2746-308_2746-306del
XM_017028302.2:c.2386-308_2386-306del	XP_016883791.1:n.2386-308_2386-306del
XM_017028303.1:c.2746-308_2746-306del	XP_016883792.1:n.2746-308_2746-306del
XM_017028304.1:c.2746-308_2746-306del	XP_016883793.1:n.2746-308_2746-306del
XM_017028305.1:c.*96-308_*96-306del	XP_016883794.1:n.*96-308_*96-306del
NM_015151.4:c.2638-308_2638-306del MANE Select	NP_055966.2:n.2638-308_2638-306del
NM_001146116.2:c.2626-308_2626-306del	NP_001139588.1:n.2626-308_2626-306del
NM_001353942.2:c.2641-308_2641-306del	NP_001340871.1:n.2641-308_2641-306del
NM_001353943.2:c.2638-308_2638-306del	NP_001340872.1:n.2638-308_2638-306del