Canonical Allele Identifier: CA1951454105

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142074_9142075delinsCT , CM000673.2:g.9142074_9142075delinsCT	GRCh38
NC_000011.9:g.9163621_9163622delinsCT , CM000673.1:g.9163621_9163622delinsCT	GRCh37
NC_000011.8:g.9120197_9120198delinsCT	NCBI36
NG_053019.1:g.128261_128262delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3545_3546delinsAG MANE Select	ENSP00000328524.3:p.Lys1182=
ENST00000525784.6:n.1407_1408delinsAG
ENST00000530780.2:c.*3371_*3372delinsAG	ENSP00000433925.1:n.*3371_*3372delinsAG
ENST00000531747.2:n.3216_3217delinsAG
ENST00000679446.1:n.3466_3467delinsAG
ENST00000679458.1:n.4946_4947delinsAG
ENST00000679460.1:n.4607_4608delinsAG
ENST00000679568.1:c.3545_3546delinsAG	ENSP00000505860.1:p.Lys1182=
ENST00000679745.1:n.4050_4051delinsAG
ENST00000679773.1:n.2706_2707delinsAG
ENST00000679926.1:n.4847_4848delinsAG
ENST00000679999.1:c.*602_*603delinsAG	ENSP00000505198.1:n.*602_*603delinsAG
ENST00000680252.1:c.3212_3213delinsAG
ENST00000680294.1:c.3338_3339delinsAG	ENSP00000506113.1:p.Lys1113=
ENST00000680358.1:n.2844_2845delinsAG
ENST00000680470.1:c.*1326_*1327delinsAG	ENSP00000505975.1:n.*1326_*1327delinsAG
ENST00000680554.1:c.*78_*79delinsAG	ENSP00000505621.1:n.*78_*79delinsAG
ENST00000680576.1:n.5021_5022delinsAG
ENST00000680599.1:n.3586_3587delinsAG
ENST00000680742.1:c.*78_*79delinsAG	ENSP00000505206.1:n.*78_*79delinsAG
ENST00000680791.1:n.2429_2430delinsAG
ENST00000680885.1:n.5247_5248delinsAG
ENST00000681158.1:c.3129_3130delinsAG
ENST00000681203.1:c.3473_3474delinsAG	ENSP00000506456.1:p.Lys1158=
ENST00000681371.1:n.3417_3418delinsAG
ENST00000681425.1:n.4023_4024delinsAG
ENST00000681639.1:n.1824_1825delinsAG
ENST00000328194.7:c.3545_3546delinsAG	ENSP00000328524.3:p.Lys1182=
ENST00000525784.5:c.481_482delinsAG
ENST00000527700.5:n.3107_3108delinsAG
ENST00000528725.5:c.241_242delinsAG
ENST00000529977.5:n.1446_1447delinsAG
ENST00000530044.5:c.3545_3546delinsAG	ENSP00000435866.1:p.Lys1182=
ENST00000531747.1:c.781_782delinsAG
ENST00000533737.5:c.208_209delinsAG
NM_001243254.1:c.3545_3546delinsAG	NP_001230183.1:p.Lys1182=
NM_015213.3:c.3545_3546delinsAG	NP_056028.2:p.Lys1182=
XM_005252832.1:c.3545_3546delinsAG	XP_005252889.1:p.Lys1182=
XM_011519952.1:c.3545_3546delinsAG	XP_011518254.1:p.Lys1182=
XM_011519953.1:c.1643_1644delinsAG	XP_011518255.1:p.Lys548=
XR_242782.2:n.3727_3728delinsAG
XR_930851.1:n.3727_3728delinsAG
NM_001348749.1:c.3473_3474delinsAG	NP_001335678.1:p.Lys1158=
NM_001348750.1:c.3257_3258delinsAG	NP_001335679.1:p.Lys1086=
NR_145966.2:n.3719_3720delinsAG
NM_015213.4:c.3545_3546delinsAG MANE Select	NP_056028.2:p.Lys1182=
NM_001243254.2:c.3545_3546delinsAG	NP_001230183.1:p.Lys1182=
NM_001348749.2:c.3473_3474delinsAG	NP_001335678.1:p.Lys1158=
NM_001348750.2:c.3257_3258delinsAG	NP_001335679.1:p.Lys1086=