Canonical Allele Identifier: CA1951492131

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204326_9204329delinsGACA , CM000673.2:g.9204326_9204329delinsGACA	GRCh38
NC_000011.9:g.9225873_9225876delinsGACA , CM000673.1:g.9225873_9225876delinsGACA	GRCh37
NC_000011.8:g.9182449_9182452delinsGACA	NCBI36
NG_053019.1:g.66007_66010delinsTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.292-12_292-9delinsTGTC MANE Select	ENSP00000328524.3:n.292-12_292-9delinsTGTC
ENST00000530780.2:c.*118-12_*118-9delinsTGTC	ENSP00000433925.1:n.*118-12_*118-9delinsTGTC
ENST00000530867.2:n.81-12_81-9delinsTGTC
ENST00000532696.2:n.215-12_215-9delinsTGTC
ENST00000679446.1:n.213-12_213-9delinsTGTC
ENST00000679460.1:n.81-12_81-9delinsTGTC
ENST00000679568.1:c.292-12_292-9delinsTGTC	ENSP00000505860.1:n.292-12_292-9delinsTGTC
ENST00000679745.1:n.81-12_81-9delinsTGTC
ENST00000679999.1:c.292-12_292-9delinsTGTC	ENSP00000505198.1:n.292-12_292-9delinsTGTC
ENST00000680252.1:c.81-12_81-9delinsTGTC
ENST00000680294.1:c.292-12_292-9delinsTGTC	ENSP00000506113.1:n.292-12_292-9delinsTGTC
ENST00000680470.1:c.292-12_292-9delinsTGTC	ENSP00000505975.1:n.292-12_292-9delinsTGTC
ENST00000680554.1:c.4-12_4-9delinsTGTC	ENSP00000505621.1:n.4-12_4-9delinsTGTC
ENST00000680576.1:n.81-12_81-9delinsTGTC
ENST00000680599.1:n.209-12_209-9delinsTGTC
ENST00000680742.1:c.292-12_292-9delinsTGTC	ENSP00000505206.1:n.292-12_292-9delinsTGTC
ENST00000680885.1:n.213-12_213-9delinsTGTC
ENST00000681158.1:c.81-12_81-9delinsTGTC
ENST00000681173.1:n.81-12_81-9delinsTGTC
ENST00000681203.1:c.220-12_220-9delinsTGTC	ENSP00000506456.1:n.220-12_220-9delinsTGTC
ENST00000681425.1:n.213-12_213-9delinsTGTC
ENST00000681915.1:n.81-12_81-9delinsTGTC
ENST00000328194.7:c.292-12_292-9delinsTGTC	ENSP00000328524.3:n.292-12_292-9delinsTGTC
ENST00000526707.5:c.220-12_220-9delinsTGTC	ENSP00000436780.1:n.220-12_220-9delinsTGTC
ENST00000530044.5:c.292-12_292-9delinsTGTC	ENSP00000435866.1:n.292-12_292-9delinsTGTC
ENST00000530780.1:c.*118-12_*118-9delinsTGTC	ENSP00000433925.1:n.*118-12_*118-9delinsTGTC
ENST00000532696.1:n.47-12_47-9delinsTGTC
NM_001243254.1:c.292-12_292-9delinsTGTC	NP_001230183.1:n.292-12_292-9delinsTGTC
NM_015213.3:c.292-12_292-9delinsTGTC	NP_056028.2:n.292-12_292-9delinsTGTC
XM_005252832.1:c.292-12_292-9delinsTGTC	XP_005252889.1:n.292-12_292-9delinsTGTC
XM_011519952.1:c.292-12_292-9delinsTGTC	XP_011518254.1:n.292-12_292-9delinsTGTC
XR_242782.2:n.557-12_557-9delinsTGTC
XR_930851.1:n.557-12_557-9delinsTGTC
XR_930852.1:n.557-12_557-9delinsTGTC
XR_930853.1:n.557-12_557-9delinsTGTC
NM_001348749.1:c.220-12_220-9delinsTGTC	NP_001335678.1:n.220-12_220-9delinsTGTC
NM_001348750.1:c.4-12_4-9delinsTGTC	NP_001335679.1:n.4-12_4-9delinsTGTC
NR_145966.2:n.549-12_549-9delinsTGTC
NM_015213.4:c.292-12_292-9delinsTGTC MANE Select	NP_056028.2:n.292-12_292-9delinsTGTC
NM_001243254.2:c.292-12_292-9delinsTGTC	NP_001230183.1:n.292-12_292-9delinsTGTC
NM_001348749.2:c.220-12_220-9delinsTGTC	NP_001335678.1:n.220-12_220-9delinsTGTC
NM_001348750.2:c.4-12_4-9delinsTGTC	NP_001335679.1:n.4-12_4-9delinsTGTC