Canonical Allele Identifier: CA1951453956

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141791_9141802delinsAGGAAATTCAGG , CM000673.2:g.9141791_9141802delinsAGGAAATTCAGG	GRCh38
NC_000011.9:g.9163338_9163349delinsAGGAAATTCAGG , CM000673.1:g.9163338_9163349delinsAGGAAATTCAGG	GRCh37
NC_000011.8:g.9119914_9119925delinsAGGAAATTCAGG	NCBI36
NG_053019.1:g.128534_128545delinsCCTGAATTTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+138_3680+149delinsCCTGAATTTCCT MANE Select	ENSP00000328524.3:n.3680+138_3680+149delinsCCTGAATTTCCT
ENST00000525784.6:n.1542+138_1542+149delinsCCTGAATTTCCT
ENST00000530780.2:c.*3506+138_*3506+149delinsCCTGAATTTCCT	ENSP00000433925.1:n.*3506+138_*3506+149delinsCCTGAATTTCCT
ENST00000531747.2:n.3351+138_3351+149delinsCCTGAATTTCCT
ENST00000679446.1:n.3739_3750delinsCCTGAATTTCCT
ENST00000679458.1:n.5081+138_5081+149delinsCCTGAATTTCCT
ENST00000679460.1:n.4742+138_4742+149delinsCCTGAATTTCCT
ENST00000679568.1:c.3680+138_3680+149delinsCCTGAATTTCCT	ENSP00000505860.1:n.3680+138_3680+149delinsCCTGAATTTCCT
ENST00000679745.1:n.4185+138_4185+149delinsCCTGAATTTCCT
ENST00000679773.1:n.2841+138_2841+149delinsCCTGAATTTCCT
ENST00000679926.1:n.4982+138_4982+149delinsCCTGAATTTCCT
ENST00000679999.1:c.*737+138_*737+149delinsCCTGAATTTCCT	ENSP00000505198.1:n.*737+138_*737+149delinsCCTGAATTTCCT
ENST00000680252.1:c.3347+138_3347+149delinsCCTGAATTTCCT
ENST00000680294.1:c.3473+138_3473+149delinsCCTGAATTTCCT	ENSP00000506113.1:n.3473+138_3473+149delinsCCTGAATTTCCT
ENST00000680358.1:n.2979+138_2979+149delinsCCTGAATTTCCT
ENST00000680470.1:c.*1461+138_*1461+149delinsCCTGAATTTCCT	ENSP00000505975.1:n.*1461+138_*1461+149delinsCCTGAATTTCCT
ENST00000680554.1:c.*213+138_*213+149delinsCCTGAATTTCCT	ENSP00000505621.1:n.*213+138_*213+149delinsCCTGAATTTCCT
ENST00000680576.1:n.5294_5305delinsCCTGAATTTCCT
ENST00000680599.1:n.3721+138_3721+149delinsCCTGAATTTCCT
ENST00000680742.1:c.*179+172_*179+183delinsCCTGAATTTCCT	ENSP00000505206.1:n.*179+172_*179+183delinsCCTGAATTTCCT
ENST00000680791.1:n.2564+138_2564+149delinsCCTGAATTTCCT
ENST00000680885.1:n.5382+138_5382+149delinsCCTGAATTTCCT
ENST00000681158.1:c.3264+138_3264+149delinsCCTGAATTTCCT
ENST00000681203.1:c.3608+138_3608+149delinsCCTGAATTTCCT	ENSP00000506456.1:n.3608+138_3608+149delinsCCTGAATTTCCT
ENST00000681371.1:n.3552+138_3552+149delinsCCTGAATTTCCT
ENST00000681425.1:n.4158+138_4158+149delinsCCTGAATTTCCT
ENST00000681639.1:n.1959+138_1959+149delinsCCTGAATTTCCT
ENST00000328194.7:c.3680+138_3680+149delinsCCTGAATTTCCT	ENSP00000328524.3:n.3680+138_3680+149delinsCCTGAATTTCCT
ENST00000525784.5:c.616+138_616+149delinsCCTGAATTTCCT
ENST00000527700.5:n.3242+138_3242+149delinsCCTGAATTTCCT
ENST00000528725.5:c.376+138_376+149delinsCCTGAATTTCCT
ENST00000529977.5:n.1581+138_1581+149delinsCCTGAATTTCCT
ENST00000530044.5:c.3646+172_3646+183delinsCCTGAATTTCCT	ENSP00000435866.1:n.3646+172_3646+183delinsCCTGAATTTCCT
ENST00000533737.5:c.343+138_343+149delinsCCTGAATTTCCT
NM_001243254.1:c.3646+172_3646+183delinsCCTGAATTTCCT	NP_001230183.1:n.3646+172_3646+183delinsCCTGAATTTCCT
NM_015213.3:c.3680+138_3680+149delinsCCTGAATTTCCT	NP_056028.2:n.3680+138_3680+149delinsCCTGAATTTCCT
XM_005252832.1:c.3680+138_3680+149delinsCCTGAATTTCCT	XP_005252889.1:n.3680+138_3680+149delinsCCTGAATTTCCT
XM_011519952.1:c.3646+172_3646+183delinsCCTGAATTTCCT	XP_011518254.1:n.3646+172_3646+183delinsCCTGAATTTCCT
XM_011519953.1:c.1778+138_1778+149delinsCCTGAATTTCCT	XP_011518255.1:n.1778+138_1778+149delinsCCTGAATTTCCT
XR_242782.2:n.3862+138_3862+149delinsCCTGAATTTCCT
XR_930851.1:n.3828+172_3828+183delinsCCTGAATTTCCT
NM_001348749.1:c.3608+138_3608+149delinsCCTGAATTTCCT	NP_001335678.1:n.3608+138_3608+149delinsCCTGAATTTCCT
NM_001348750.1:c.3392+138_3392+149delinsCCTGAATTTCCT	NP_001335679.1:n.3392+138_3392+149delinsCCTGAATTTCCT
NR_145966.2:n.3854+138_3854+149delinsCCTGAATTTCCT
NM_015213.4:c.3680+138_3680+149delinsCCTGAATTTCCT MANE Select	NP_056028.2:n.3680+138_3680+149delinsCCTGAATTTCCT
NM_001243254.2:c.3646+172_3646+183delinsCCTGAATTTCCT	NP_001230183.1:n.3646+172_3646+183delinsCCTGAATTTCCT
NM_001348749.2:c.3608+138_3608+149delinsCCTGAATTTCCT	NP_001335678.1:n.3608+138_3608+149delinsCCTGAATTTCCT
NM_001348750.2:c.3392+138_3392+149delinsCCTGAATTTCCT	NP_001335679.1:n.3392+138_3392+149delinsCCTGAATTTCCT