Canonical Allele Identifier: CA1951454058

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141972_9141973delinsGC , CM000673.2:g.9141972_9141973delinsGC	GRCh38
NC_000011.9:g.9163519_9163520delinsGC , CM000673.1:g.9163519_9163520delinsGC	GRCh37
NC_000011.8:g.9120095_9120096delinsGC	NCBI36
NG_053019.1:g.128363_128364delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3647_3648delinsGC MANE Select	ENSP00000328524.3:p.Gly1216=
ENST00000525784.6:n.1509_1510delinsGC
ENST00000530780.2:c.*3473_*3474delinsGC	ENSP00000433925.1:n.*3473_*3474delinsGC
ENST00000531747.2:n.3318_3319delinsGC
ENST00000679446.1:n.3568_3569delinsGC
ENST00000679458.1:n.5048_5049delinsGC
ENST00000679460.1:n.4709_4710delinsGC
ENST00000679568.1:c.3647_3648delinsGC	ENSP00000505860.1:p.Gly1216=
ENST00000679745.1:n.4152_4153delinsGC
ENST00000679773.1:n.2808_2809delinsGC
ENST00000679926.1:n.4949_4950delinsGC
ENST00000679999.1:c.*704_*705delinsGC	ENSP00000505198.1:n.*704_*705delinsGC
ENST00000680252.1:c.3314_3315delinsGC
ENST00000680294.1:c.3440_3441delinsGC	ENSP00000506113.1:p.Gly1147=
ENST00000680358.1:n.2946_2947delinsGC
ENST00000680470.1:c.*1428_*1429delinsGC	ENSP00000505975.1:n.*1428_*1429delinsGC
ENST00000680554.1:c.*180_*181delinsGC	ENSP00000505621.1:n.*180_*181delinsGC
ENST00000680576.1:n.5123_5124delinsGC
ENST00000680599.1:n.3688_3689delinsGC
ENST00000680742.1:c.*179+1_*179+2delinsGC	ENSP00000505206.1:n.*179+1_*179+2delinsGC
ENST00000680791.1:n.2531_2532delinsGC
ENST00000680885.1:n.5349_5350delinsGC
ENST00000681158.1:c.3231_3232delinsGC
ENST00000681203.1:c.3575_3576delinsGC	ENSP00000506456.1:p.Gly1192=
ENST00000681371.1:n.3519_3520delinsGC
ENST00000681425.1:n.4125_4126delinsGC
ENST00000681639.1:n.1926_1927delinsGC
ENST00000328194.7:c.3647_3648delinsGC	ENSP00000328524.3:p.Gly1216=
ENST00000525784.5:c.583_584delinsGC
ENST00000527700.5:n.3209_3210delinsGC
ENST00000528725.5:c.343_344delinsGC
ENST00000529977.5:n.1548_1549delinsGC
ENST00000530044.5:c.3646+1_3646+2delinsGC	ENSP00000435866.1:n.3646+1_3646+2delinsGC
ENST00000531747.1:c.883_884delinsGC
ENST00000533737.5:c.310_311delinsGC
NM_001243254.1:c.3646+1_3646+2delinsGC	NP_001230183.1:n.3646+1_3646+2delinsGC
NM_015213.3:c.3647_3648delinsGC	NP_056028.2:p.Gly1216=
XM_005252832.1:c.3647_3648delinsGC	XP_005252889.1:p.Gly1216=
XM_011519952.1:c.3646+1_3646+2delinsGC	XP_011518254.1:n.3646+1_3646+2delinsGC
XM_011519953.1:c.1745_1746delinsGC	XP_011518255.1:p.Gly582=
XR_242782.2:n.3829_3830delinsGC
XR_930851.1:n.3828+1_3828+2delinsGC
NM_001348749.1:c.3575_3576delinsGC	NP_001335678.1:p.Gly1192=
NM_001348750.1:c.3359_3360delinsGC	NP_001335679.1:p.Gly1120=
NR_145966.2:n.3821_3822delinsGC
NM_015213.4:c.3647_3648delinsGC MANE Select	NP_056028.2:p.Gly1216=
NM_001243254.2:c.3646+1_3646+2delinsGC	NP_001230183.1:n.3646+1_3646+2delinsGC
NM_001348749.2:c.3575_3576delinsGC	NP_001335678.1:p.Gly1192=
NM_001348750.2:c.3359_3360delinsGC	NP_001335679.1:p.Gly1120=