Canonical Allele Identifier: CA2818115587

Gene: DIP2A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46550135_46550142del , CM000683.2:g.46550135_46550142del	GRCh38
NC_000021.8:g.47970048_47970055del , CM000683.1:g.47970048_47970055del	GRCh37
NC_000021.7:g.46794476_46794483del	NCBI36
NG_015996.1:g.96187_96194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417564.3:c.2637+250_2637+257del MANE Select	ENSP00000392066.2:n.2637+250_2637+257del
ENST00000651436.1:c.2637+250_2637+257del	ENSP00000498874.1:n.2637+250_2637+257del
ENST00000400274.5:c.2625+250_2625+257del	ENSP00000383133.1:n.2625+250_2625+257del
ENST00000417564.2:c.2637+250_2637+257del	ENSP00000392066.2:n.2637+250_2637+257del
NM_001146116.1:c.2625+250_2625+257del	NP_001139588.1:n.2625+250_2625+257del
NM_015151.3:c.2637+250_2637+257del	NP_055966.2:n.2637+250_2637+257del
XM_011529488.1:c.2745+250_2745+257del	XP_011527790.1:n.2745+250_2745+257del
XM_011529489.1:c.2745+250_2745+257del	XP_011527791.1:n.2745+250_2745+257del
XM_011529490.1:c.2745+250_2745+257del	XP_011527792.1:n.2745+250_2745+257del
XM_011529491.1:c.2742+250_2742+257del	XP_011527793.1:n.2742+250_2742+257del
XM_011529492.1:c.2745+250_2745+257del	XP_011527794.1:n.2745+250_2745+257del
XM_011529493.1:c.2640+250_2640+257del	XP_011527795.1:n.2640+250_2640+257del
XM_011529494.1:c.2637+250_2637+257del	XP_011527796.1:n.2637+250_2637+257del
XM_011529495.1:c.2613+250_2613+257del	XP_011527797.1:n.2613+250_2613+257del
XM_011529496.1:c.2490+250_2490+257del	XP_011527798.1:n.2490+250_2490+257del
XM_011529497.1:c.2745+250_2745+257del	XP_011527799.1:n.2745+250_2745+257del
XM_011529498.1:c.2745+250_2745+257del	XP_011527800.1:n.2745+250_2745+257del
XM_011529499.1:c.2745+250_2745+257del	XP_011527801.1:n.2745+250_2745+257del
XM_011529500.1:c.2745+250_2745+257del	XP_011527802.1:n.2745+250_2745+257del
XM_011529501.1:c.2745+250_2745+257del	XP_011527803.1:n.2745+250_2745+257del
NM_001353942.1:c.2640+250_2640+257del	NP_001340871.1:n.2640+250_2640+257del
NM_001353943.1:c.2637+250_2637+257del	NP_001340872.1:n.2637+250_2637+257del
XM_011529492.2:c.2745+250_2745+257del	XP_011527794.1:n.2745+250_2745+257del
XM_017028291.1:c.2745+250_2745+257del	XP_016883780.1:n.2745+250_2745+257del
XM_017028292.1:c.2745+250_2745+257del	XP_016883781.1:n.2745+250_2745+257del
XM_017028293.1:c.2742+250_2742+257del	XP_016883782.1:n.2742+250_2742+257del
XM_017028294.2:c.2640+250_2640+257del	XP_016883783.1:n.2640+250_2640+257del
XM_017028295.2:c.2637+250_2637+257del	XP_016883784.1:n.2637+250_2637+257del
XM_017028297.1:c.2613+250_2613+257del	XP_016883786.1:n.2613+250_2613+257del
XM_017028298.2:c.2508+250_2508+257del	XP_016883787.1:n.2508+250_2508+257del
XM_017028299.1:c.2490+250_2490+257del	XP_016883788.1:n.2490+250_2490+257del
XM_017028300.1:c.2745+250_2745+257del	XP_016883789.1:n.2745+250_2745+257del
XM_017028301.1:c.2745+250_2745+257del	XP_016883790.1:n.2745+250_2745+257del
XM_017028302.2:c.2385+250_2385+257del	XP_016883791.1:n.2385+250_2385+257del
XM_017028303.1:c.2745+250_2745+257del	XP_016883792.1:n.2745+250_2745+257del
XM_017028304.1:c.2745+250_2745+257del	XP_016883793.1:n.2745+250_2745+257del
XM_017028305.1:c.*95+250_*95+257del	XP_016883794.1:n.*95+250_*95+257del
NM_015151.4:c.2637+250_2637+257del MANE Select	NP_055966.2:n.2637+250_2637+257del
NM_001146116.2:c.2625+250_2625+257del	NP_001139588.1:n.2625+250_2625+257del
NM_001353942.2:c.2640+250_2640+257del	NP_001340871.1:n.2640+250_2640+257del
NM_001353943.2:c.2637+250_2637+257del	NP_001340872.1:n.2637+250_2637+257del