Canonical Allele Identifier: CA410571326

Gene: DIP2A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46533649T>G , CM000683.2:g.46533649T>G	GRCh38
NC_000021.8:g.47953562T>G , CM000683.1:g.47953562T>G	GRCh37
NC_000021.7:g.46777990T>G	NCBI36
NG_015996.1:g.79701T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015151.4:c.1429+2T>G MANE Select	NP_055966.2:n.1429+2T>G
ENST00000417564.3:c.1429+2T>G MANE Select	ENSP00000392066.2:n.1429+2T>G
NM_001146115.1:c.1300+2T>G	NP_001139587.1:n.1300+2T>G
NM_001146115.2:c.1300+2T>G	NP_001139587.1:n.1300+2T>G
NM_001146116.1:c.1417+2T>G	NP_001139588.1:n.1417+2T>G
NM_001146116.2:c.1417+2T>G	NP_001139588.1:n.1417+2T>G
NM_001353942.1:c.1432+2T>G	NP_001340871.1:n.1432+2T>G
NM_001353942.2:c.1432+2T>G	NP_001340871.1:n.1432+2T>G
NM_001353943.1:c.1429+2T>G	NP_001340872.1:n.1429+2T>G
NM_001353943.2:c.1429+2T>G	NP_001340872.1:n.1429+2T>G
NM_001353944.1:c.1180+2T>G	NP_001340873.1:n.1180+2T>G
NM_001353944.2:c.1180+2T>G	NP_001340873.1:n.1180+2T>G
NM_015151.3:c.1429+2T>G	NP_055966.2:n.1429+2T>G
NM_206889.2:c.1429+2T>G	NP_996772.1:n.1429+2T>G
NM_206889.3:c.1429+2T>G	NP_996772.1:n.1429+2T>G
NM_206890.2:c.1429+2T>G	NP_996773.1:n.1429+2T>G
NM_206890.3:c.1429+2T>G	NP_996773.1:n.1429+2T>G
NM_206891.2:c.1429+2T>G	NP_996774.1:n.1429+2T>G
NM_206891.3:c.1429+2T>G	NP_996774.1:n.1429+2T>G
ENST00000400274.5:c.1417+2T>G	ENSP00000383133.1:n.1417+2T>G
ENST00000417564.2:c.1429+2T>G	ENSP00000392066.2:n.1429+2T>G
ENST00000435722.7:c.1429+2T>G	ENSP00000415089.3:n.1429+2T>G
ENST00000457905.7:c.1429+2T>G	ENSP00000393434.3:n.1429+2T>G
ENST00000466639.5:c.1300+2T>G	ENSP00000430249.1:n.1300+2T>G
ENST00000473752.5:n.822+2T>G
ENST00000494435.5:n.755+2T>G
ENST00000651436.1:c.1429+2T>G	ENSP00000498874.1:n.1429+2T>G
XM_011529488.1:c.1537+2T>G	XP_011527790.1:n.1537+2T>G
XM_011529489.1:c.1537+2T>G	XP_011527791.1:n.1537+2T>G
XM_011529490.1:c.1537+2T>G	XP_011527792.1:n.1537+2T>G
XM_011529491.1:c.1534+2T>G	XP_011527793.1:n.1534+2T>G
XM_011529492.1:c.1537+2T>G	XP_011527794.1:n.1537+2T>G
XM_011529492.2:c.1537+2T>G	XP_011527794.1:n.1537+2T>G
XM_011529493.1:c.1432+2T>G	XP_011527795.1:n.1432+2T>G
XM_011529494.1:c.1429+2T>G	XP_011527796.1:n.1429+2T>G
XM_011529495.1:c.1405+2T>G	XP_011527797.1:n.1405+2T>G
XM_011529496.1:c.1282+2T>G	XP_011527798.1:n.1282+2T>G
XM_011529497.1:c.1537+2T>G	XP_011527799.1:n.1537+2T>G
XM_011529498.1:c.1537+2T>G	XP_011527800.1:n.1537+2T>G
XM_011529499.1:c.1537+2T>G	XP_011527801.1:n.1537+2T>G
XM_011529500.1:c.1537+2T>G	XP_011527802.1:n.1537+2T>G
XM_011529501.1:c.1537+2T>G	XP_011527803.1:n.1537+2T>G
XM_011529502.1:c.1537+2T>G	XP_011527804.1:n.1537+2T>G
XM_011529503.1:c.1537+2T>G	XP_011527805.1:n.1537+2T>G
XM_017028291.1:c.1537+2T>G	XP_016883780.1:n.1537+2T>G
XM_017028292.1:c.1537+2T>G	XP_016883781.1:n.1537+2T>G
XM_017028293.1:c.1534+2T>G	XP_016883782.1:n.1534+2T>G
XM_017028294.2:c.1432+2T>G	XP_016883783.1:n.1432+2T>G
XM_017028295.2:c.1429+2T>G	XP_016883784.1:n.1429+2T>G
XM_017028297.1:c.1405+2T>G	XP_016883786.1:n.1405+2T>G
XM_017028298.2:c.1300+2T>G	XP_016883787.1:n.1300+2T>G
XM_017028299.1:c.1282+2T>G	XP_016883788.1:n.1282+2T>G
XM_017028300.1:c.1537+2T>G	XP_016883789.1:n.1537+2T>G
XM_017028301.1:c.1537+2T>G	XP_016883790.1:n.1537+2T>G
XM_017028302.2:c.1177+2T>G	XP_016883791.1:n.1177+2T>G
XM_017028303.1:c.1537+2T>G	XP_016883792.1:n.1537+2T>G
XM_017028304.1:c.1537+2T>G	XP_016883793.1:n.1537+2T>G
XM_017028305.1:c.1537+2T>G	XP_016883794.1:n.1537+2T>G