Canonical Allele Identifier: CA1951453992

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141862_9141863delinsAC , CM000673.2:g.9141862_9141863delinsAC	GRCh38
NC_000011.9:g.9163409_9163410delinsAC , CM000673.1:g.9163409_9163410delinsAC	GRCh37
NC_000011.8:g.9119985_9119986delinsAC	NCBI36
NG_053019.1:g.128473_128474delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+77_3680+78delinsGT MANE Select	ENSP00000328524.3:n.3680+77_3680+78delinsGT
ENST00000525784.6:n.1542+77_1542+78delinsGT
ENST00000530780.2:c.*3506+77_*3506+78delinsGT	ENSP00000433925.1:n.*3506+77_*3506+78delinsGT
ENST00000531747.2:n.3351+77_3351+78delinsGT
ENST00000679446.1:n.3678_3679delinsGT
ENST00000679458.1:n.5081+77_5081+78delinsGT
ENST00000679460.1:n.4742+77_4742+78delinsGT
ENST00000679568.1:c.3680+77_3680+78delinsGT	ENSP00000505860.1:n.3680+77_3680+78delinsGT
ENST00000679745.1:n.4185+77_4185+78delinsGT
ENST00000679773.1:n.2841+77_2841+78delinsGT
ENST00000679926.1:n.4982+77_4982+78delinsGT
ENST00000679999.1:c.*737+77_*737+78delinsGT	ENSP00000505198.1:n.*737+77_*737+78delinsGT
ENST00000680252.1:c.3347+77_3347+78delinsGT
ENST00000680294.1:c.3473+77_3473+78delinsGT	ENSP00000506113.1:n.3473+77_3473+78delinsGT
ENST00000680358.1:n.2979+77_2979+78delinsGT
ENST00000680470.1:c.*1461+77_*1461+78delinsGT	ENSP00000505975.1:n.*1461+77_*1461+78delinsGT
ENST00000680554.1:c.*213+77_*213+78delinsGT	ENSP00000505621.1:n.*213+77_*213+78delinsGT
ENST00000680576.1:n.5233_5234delinsGT
ENST00000680599.1:n.3721+77_3721+78delinsGT
ENST00000680742.1:c.*179+111_*179+112delinsGT	ENSP00000505206.1:n.*179+111_*179+112delinsGT
ENST00000680791.1:n.2564+77_2564+78delinsGT
ENST00000680885.1:n.5382+77_5382+78delinsGT
ENST00000681158.1:c.3264+77_3264+78delinsGT
ENST00000681203.1:c.3608+77_3608+78delinsGT	ENSP00000506456.1:n.3608+77_3608+78delinsGT
ENST00000681371.1:n.3552+77_3552+78delinsGT
ENST00000681425.1:n.4158+77_4158+78delinsGT
ENST00000681639.1:n.1959+77_1959+78delinsGT
ENST00000328194.7:c.3680+77_3680+78delinsGT	ENSP00000328524.3:n.3680+77_3680+78delinsGT
ENST00000525784.5:c.616+77_616+78delinsGT
ENST00000527700.5:n.3242+77_3242+78delinsGT
ENST00000528725.5:c.376+77_376+78delinsGT
ENST00000529977.5:n.1581+77_1581+78delinsGT
ENST00000530044.5:c.3646+111_3646+112delinsGT	ENSP00000435866.1:n.3646+111_3646+112delinsGT
ENST00000533737.5:c.343+77_343+78delinsGT
NM_001243254.1:c.3646+111_3646+112delinsGT	NP_001230183.1:n.3646+111_3646+112delinsGT
NM_015213.3:c.3680+77_3680+78delinsGT	NP_056028.2:n.3680+77_3680+78delinsGT
XM_005252832.1:c.3680+77_3680+78delinsGT	XP_005252889.1:n.3680+77_3680+78delinsGT
XM_011519952.1:c.3646+111_3646+112delinsGT	XP_011518254.1:n.3646+111_3646+112delinsGT
XM_011519953.1:c.1778+77_1778+78delinsGT	XP_011518255.1:n.1778+77_1778+78delinsGT
XR_242782.2:n.3862+77_3862+78delinsGT
XR_930851.1:n.3828+111_3828+112delinsGT
NM_001348749.1:c.3608+77_3608+78delinsGT	NP_001335678.1:n.3608+77_3608+78delinsGT
NM_001348750.1:c.3392+77_3392+78delinsGT	NP_001335679.1:n.3392+77_3392+78delinsGT
NR_145966.2:n.3854+77_3854+78delinsGT
NM_015213.4:c.3680+77_3680+78delinsGT MANE Select	NP_056028.2:n.3680+77_3680+78delinsGT
NM_001243254.2:c.3646+111_3646+112delinsGT	NP_001230183.1:n.3646+111_3646+112delinsGT
NM_001348749.2:c.3608+77_3608+78delinsGT	NP_001335678.1:n.3608+77_3608+78delinsGT
NM_001348750.2:c.3392+77_3392+78delinsGT	NP_001335679.1:n.3392+77_3392+78delinsGT