Canonical Allele Identifier: CA1951492189

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204430_9204431delinsTG , CM000673.2:g.9204430_9204431delinsTG	GRCh38
NC_000011.9:g.9225977_9225978delinsTG , CM000673.1:g.9225977_9225978delinsTG	GRCh37
NC_000011.8:g.9182553_9182554delinsTG	NCBI36
NG_053019.1:g.65905_65906delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.292-114_292-113delinsCA MANE Select	ENSP00000328524.3:n.292-114_292-113delinsCA
ENST00000530780.2:c.*118-114_*118-113delinsCA	ENSP00000433925.1:n.*118-114_*118-113delinsCA
ENST00000530867.2:n.81-114_81-113delinsCA
ENST00000532696.2:n.215-114_215-113delinsCA
ENST00000679446.1:n.213-114_213-113delinsCA
ENST00000679460.1:n.81-114_81-113delinsCA
ENST00000679568.1:c.292-114_292-113delinsCA	ENSP00000505860.1:n.292-114_292-113delinsCA
ENST00000679745.1:n.81-114_81-113delinsCA
ENST00000679999.1:c.292-114_292-113delinsCA	ENSP00000505198.1:n.292-114_292-113delinsCA
ENST00000680252.1:c.81-114_81-113delinsCA
ENST00000680294.1:c.292-114_292-113delinsCA	ENSP00000506113.1:n.292-114_292-113delinsCA
ENST00000680470.1:c.292-114_292-113delinsCA	ENSP00000505975.1:n.292-114_292-113delinsCA
ENST00000680554.1:c.4-114_4-113delinsCA	ENSP00000505621.1:n.4-114_4-113delinsCA
ENST00000680576.1:n.81-114_81-113delinsCA
ENST00000680599.1:n.209-114_209-113delinsCA
ENST00000680742.1:c.292-114_292-113delinsCA	ENSP00000505206.1:n.292-114_292-113delinsCA
ENST00000680885.1:n.213-114_213-113delinsCA
ENST00000681158.1:c.81-114_81-113delinsCA
ENST00000681173.1:n.81-114_81-113delinsCA
ENST00000681203.1:c.220-114_220-113delinsCA	ENSP00000506456.1:n.220-114_220-113delinsCA
ENST00000681425.1:n.213-114_213-113delinsCA
ENST00000681915.1:n.81-114_81-113delinsCA
ENST00000328194.7:c.292-114_292-113delinsCA	ENSP00000328524.3:n.292-114_292-113delinsCA
ENST00000526707.5:c.220-114_220-113delinsCA	ENSP00000436780.1:n.220-114_220-113delinsCA
ENST00000530044.5:c.292-114_292-113delinsCA	ENSP00000435866.1:n.292-114_292-113delinsCA
ENST00000530780.1:c.*118-114_*118-113delinsCA	ENSP00000433925.1:n.*118-114_*118-113delinsCA
ENST00000532696.1:n.47-114_47-113delinsCA
NM_001243254.1:c.292-114_292-113delinsCA	NP_001230183.1:n.292-114_292-113delinsCA
NM_015213.3:c.292-114_292-113delinsCA	NP_056028.2:n.292-114_292-113delinsCA
XM_005252832.1:c.292-114_292-113delinsCA	XP_005252889.1:n.292-114_292-113delinsCA
XM_011519952.1:c.292-114_292-113delinsCA	XP_011518254.1:n.292-114_292-113delinsCA
XR_242782.2:n.557-114_557-113delinsCA
XR_930851.1:n.557-114_557-113delinsCA
XR_930852.1:n.557-114_557-113delinsCA
XR_930853.1:n.557-114_557-113delinsCA
NM_001348749.1:c.220-114_220-113delinsCA	NP_001335678.1:n.220-114_220-113delinsCA
NM_001348750.1:c.4-114_4-113delinsCA	NP_001335679.1:n.4-114_4-113delinsCA
NR_145966.2:n.549-114_549-113delinsCA
NM_015213.4:c.292-114_292-113delinsCA MANE Select	NP_056028.2:n.292-114_292-113delinsCA
NM_001243254.2:c.292-114_292-113delinsCA	NP_001230183.1:n.292-114_292-113delinsCA
NM_001348749.2:c.220-114_220-113delinsCA	NP_001335678.1:n.220-114_220-113delinsCA
NM_001348750.2:c.4-114_4-113delinsCA	NP_001335679.1:n.4-114_4-113delinsCA