Canonical Allele Identifier: CA2612405462
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204373_9204374insG , CM000673.2:g.9204373_9204374insG GRCh38
NC_000011.9:g.9225920_9225921insG , CM000673.1:g.9225920_9225921insG GRCh37
NC_000011.8:g.9182496_9182497insG NCBI36
NG_053019.1:g.65962_65963insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.292-57_292-56insC MANE Select ENSP00000328524.3:n.292-57_292-56insC
ENST00000530780.2:c.*118-57_*118-56insC ENSP00000433925.1:n.*118-57_*118-56insC
ENST00000530867.2:n.81-57_81-56insC
ENST00000532696.2:n.215-57_215-56insC
ENST00000679446.1:n.213-57_213-56insC
ENST00000679460.1:n.81-57_81-56insC
ENST00000679568.1:c.292-57_292-56insC ENSP00000505860.1:n.292-57_292-56insC
ENST00000679745.1:n.81-57_81-56insC
ENST00000679999.1:c.292-57_292-56insC ENSP00000505198.1:n.292-57_292-56insC
ENST00000680252.1:c.81-57_81-56insC
ENST00000680294.1:c.292-57_292-56insC ENSP00000506113.1:n.292-57_292-56insC
ENST00000680470.1:c.292-57_292-56insC ENSP00000505975.1:n.292-57_292-56insC
ENST00000680554.1:c.4-57_4-56insC ENSP00000505621.1:n.4-57_4-56insC
ENST00000680576.1:n.81-57_81-56insC
ENST00000680599.1:n.209-57_209-56insC
ENST00000680742.1:c.292-57_292-56insC ENSP00000505206.1:n.292-57_292-56insC
ENST00000680885.1:n.213-57_213-56insC
ENST00000681158.1:c.81-57_81-56insC
ENST00000681173.1:n.81-57_81-56insC
ENST00000681203.1:c.220-57_220-56insC ENSP00000506456.1:n.220-57_220-56insC
ENST00000681425.1:n.213-57_213-56insC
ENST00000681915.1:n.81-57_81-56insC
ENST00000328194.7:c.292-57_292-56insC ENSP00000328524.3:n.292-57_292-56insC
ENST00000526707.5:c.220-57_220-56insC ENSP00000436780.1:n.220-57_220-56insC
ENST00000530044.5:c.292-57_292-56insC ENSP00000435866.1:n.292-57_292-56insC
ENST00000530780.1:c.*118-57_*118-56insC ENSP00000433925.1:n.*118-57_*118-56insC
ENST00000532696.1:n.47-57_47-56insC
NM_001243254.1:c.292-57_292-56insC NP_001230183.1:n.292-57_292-56insC
NM_015213.3:c.292-57_292-56insC NP_056028.2:n.292-57_292-56insC
XM_005252832.1:c.292-57_292-56insC XP_005252889.1:n.292-57_292-56insC
XM_011519952.1:c.292-57_292-56insC XP_011518254.1:n.292-57_292-56insC
XR_242782.2:n.557-57_557-56insC
XR_930851.1:n.557-57_557-56insC
XR_930852.1:n.557-57_557-56insC
XR_930853.1:n.557-57_557-56insC
NM_001348749.1:c.220-57_220-56insC NP_001335678.1:n.220-57_220-56insC
NM_001348750.1:c.4-57_4-56insC NP_001335679.1:n.4-57_4-56insC
NR_145966.2:n.549-57_549-56insC
NM_015213.4:c.292-57_292-56insC MANE Select NP_056028.2:n.292-57_292-56insC
NM_001243254.2:c.292-57_292-56insC NP_001230183.1:n.292-57_292-56insC
NM_001348749.2:c.220-57_220-56insC NP_001335678.1:n.220-57_220-56insC
NM_001348750.2:c.4-57_4-56insC NP_001335679.1:n.4-57_4-56insC