Canonical Allele Identifier: CA1951492203

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204454_9204455delinsTG , CM000673.2:g.9204454_9204455delinsTG	GRCh38
NC_000011.9:g.9226001_9226002delinsTG , CM000673.1:g.9226001_9226002delinsTG	GRCh37
NC_000011.8:g.9182577_9182578delinsTG	NCBI36
NG_053019.1:g.65881_65882delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.292-138_292-137delinsCA MANE Select	ENSP00000328524.3:n.292-138_292-137delinsCA
ENST00000530780.2:c.*118-138_*118-137delinsCA	ENSP00000433925.1:n.*118-138_*118-137delinsCA
ENST00000530867.2:n.81-138_81-137delinsCA
ENST00000532696.2:n.215-138_215-137delinsCA
ENST00000679446.1:n.213-138_213-137delinsCA
ENST00000679460.1:n.81-138_81-137delinsCA
ENST00000679568.1:c.292-138_292-137delinsCA	ENSP00000505860.1:n.292-138_292-137delinsCA
ENST00000679745.1:n.81-138_81-137delinsCA
ENST00000679999.1:c.292-138_292-137delinsCA	ENSP00000505198.1:n.292-138_292-137delinsCA
ENST00000680252.1:c.81-138_81-137delinsCA
ENST00000680294.1:c.292-138_292-137delinsCA	ENSP00000506113.1:n.292-138_292-137delinsCA
ENST00000680470.1:c.292-138_292-137delinsCA	ENSP00000505975.1:n.292-138_292-137delinsCA
ENST00000680554.1:c.4-138_4-137delinsCA	ENSP00000505621.1:n.4-138_4-137delinsCA
ENST00000680576.1:n.81-138_81-137delinsCA
ENST00000680599.1:n.209-138_209-137delinsCA
ENST00000680742.1:c.292-138_292-137delinsCA	ENSP00000505206.1:n.292-138_292-137delinsCA
ENST00000680885.1:n.213-138_213-137delinsCA
ENST00000681158.1:c.81-138_81-137delinsCA
ENST00000681173.1:n.81-138_81-137delinsCA
ENST00000681203.1:c.220-138_220-137delinsCA	ENSP00000506456.1:n.220-138_220-137delinsCA
ENST00000681425.1:n.213-138_213-137delinsCA
ENST00000681915.1:n.81-138_81-137delinsCA
ENST00000328194.7:c.292-138_292-137delinsCA	ENSP00000328524.3:n.292-138_292-137delinsCA
ENST00000526707.5:c.220-138_220-137delinsCA	ENSP00000436780.1:n.220-138_220-137delinsCA
ENST00000530044.5:c.292-138_292-137delinsCA	ENSP00000435866.1:n.292-138_292-137delinsCA
ENST00000530780.1:c.*118-138_*118-137delinsCA	ENSP00000433925.1:n.*118-138_*118-137delinsCA
ENST00000532696.1:n.47-138_47-137delinsCA
NM_001243254.1:c.292-138_292-137delinsCA	NP_001230183.1:n.292-138_292-137delinsCA
NM_015213.3:c.292-138_292-137delinsCA	NP_056028.2:n.292-138_292-137delinsCA
XM_005252832.1:c.292-138_292-137delinsCA	XP_005252889.1:n.292-138_292-137delinsCA
XM_011519952.1:c.292-138_292-137delinsCA	XP_011518254.1:n.292-138_292-137delinsCA
XR_242782.2:n.557-138_557-137delinsCA
XR_930851.1:n.557-138_557-137delinsCA
XR_930852.1:n.557-138_557-137delinsCA
XR_930853.1:n.557-138_557-137delinsCA
NM_001348749.1:c.220-138_220-137delinsCA	NP_001335678.1:n.220-138_220-137delinsCA
NM_001348750.1:c.4-138_4-137delinsCA	NP_001335679.1:n.4-138_4-137delinsCA
NR_145966.2:n.549-138_549-137delinsCA
NM_015213.4:c.292-138_292-137delinsCA MANE Select	NP_056028.2:n.292-138_292-137delinsCA
NM_001243254.2:c.292-138_292-137delinsCA	NP_001230183.1:n.292-138_292-137delinsCA
NM_001348749.2:c.220-138_220-137delinsCA	NP_001335678.1:n.220-138_220-137delinsCA
NM_001348750.2:c.4-138_4-137delinsCA	NP_001335679.1:n.4-138_4-137delinsCA