Canonical Allele Identifier: CA379598492
Gene: DENND5A HGNC NCBI

Linked Data

gnomAD v4: 11-9203945-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9203945C>A , CM000673.2:g.9203945C>A GRCh38
NC_000011.9:g.9225492C>A , CM000673.1:g.9225492C>A GRCh37
NC_000011.8:g.9182068C>A NCBI36
NG_053019.1:g.66391G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.664G>T MANE Select ENSP00000328524.3:p.Val222Leu
ENST00000530780.2:c.*490G>T ENSP00000433925.1:n.*490G>T
ENST00000530867.2:n.453G>T
ENST00000532696.2:n.587G>T
ENST00000679446.1:n.585G>T
ENST00000679460.1:n.453G>T
ENST00000679568.1:c.664G>T ENSP00000505860.1:p.Val222Leu
ENST00000679745.1:n.453G>T
ENST00000679999.1:c.664G>T ENSP00000505198.1:p.Val222Leu
ENST00000680252.1:c.453G>T
ENST00000680294.1:c.664G>T ENSP00000506113.1:p.Val222Leu
ENST00000680470.1:c.664G>T ENSP00000505975.1:p.Val222Leu
ENST00000680554.1:c.376G>T ENSP00000505621.1:p.Val126Leu
ENST00000680576.1:n.453G>T
ENST00000680599.1:n.581G>T
ENST00000680742.1:c.664G>T ENSP00000505206.1:p.Val222Leu
ENST00000680885.1:n.585G>T
ENST00000681158.1:c.453G>T
ENST00000681173.1:n.453G>T
ENST00000681203.1:c.592G>T ENSP00000506456.1:p.Val198Leu
ENST00000681425.1:n.585G>T
ENST00000681915.1:n.453G>T
ENST00000328194.7:c.664G>T ENSP00000328524.3:p.Val222Leu
ENST00000526707.5:c.592G>T ENSP00000436780.1:p.Val198Leu
ENST00000530044.5:c.664G>T ENSP00000435866.1:p.Val222Leu
ENST00000532696.1:n.419G>T
NM_001243254.1:c.664G>T NP_001230183.1:p.Val222Leu
NM_015213.3:c.664G>T NP_056028.2:p.Val222Leu
XM_005252832.1:c.664G>T XP_005252889.1:p.Val222Leu
XM_011519952.1:c.664G>T XP_011518254.1:p.Val222Leu
XR_242782.2:n.929G>T
XR_930851.1:n.929G>T
XR_930852.1:n.929G>T
XR_930853.1:n.929G>T
NM_001348749.1:c.592G>T NP_001335678.1:p.Val198Leu
NM_001348750.1:c.376G>T NP_001335679.1:p.Val126Leu
NR_145966.2:n.921G>T
NM_015213.4:c.664G>T MANE Select NP_056028.2:p.Val222Leu
NM_001243254.2:c.664G>T NP_001230183.1:p.Val222Leu
NM_001348749.2:c.592G>T NP_001335678.1:p.Val198Leu
NM_001348750.2:c.376G>T NP_001335679.1:p.Val126Leu