Canonical Allele Identifier: CA379597098

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163490G>C (hg19) ; chr11:g.9141943G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141943G>C , CM000673.2:g.9141943G>C	GRCh38
NC_000011.9:g.9163490G>C , CM000673.1:g.9163490G>C	GRCh37
NC_000011.8:g.9120066G>C	NCBI36
NG_053019.1:g.128393C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3677C>G MANE Select	ENSP00000328524.3:p.Ala1226Gly
ENST00000525784.6:n.1539C>G
ENST00000530780.2:c.*3503C>G	ENSP00000433925.1:n.*3503C>G
ENST00000531747.2:n.3348C>G
ENST00000679446.1:n.3598C>G
ENST00000679458.1:n.5078C>G
ENST00000679460.1:n.4739C>G
ENST00000679568.1:c.3677C>G	ENSP00000505860.1:p.Ala1226Gly
ENST00000679745.1:n.4182C>G
ENST00000679773.1:n.2838C>G
ENST00000679926.1:n.4979C>G
ENST00000679999.1:c.*734C>G	ENSP00000505198.1:n.*734C>G
ENST00000680252.1:c.3344C>G
ENST00000680294.1:c.3470C>G	ENSP00000506113.1:p.Ala1157Gly
ENST00000680358.1:n.2976C>G
ENST00000680470.1:c.*1458C>G	ENSP00000505975.1:n.*1458C>G
ENST00000680554.1:c.*210C>G	ENSP00000505621.1:n.*210C>G
ENST00000680576.1:n.5153C>G
ENST00000680599.1:n.3718C>G
ENST00000680742.1:c.*179+31C>G	ENSP00000505206.1:n.*179+31C>G
ENST00000680791.1:n.2561C>G
ENST00000680885.1:n.5379C>G
ENST00000681158.1:c.3261C>G
ENST00000681203.1:c.3605C>G	ENSP00000506456.1:p.Ala1202Gly
ENST00000681371.1:n.3549C>G
ENST00000681425.1:n.4155C>G
ENST00000681639.1:n.1956C>G
ENST00000328194.7:c.3677C>G	ENSP00000328524.3:p.Ala1226Gly
ENST00000525784.5:c.613C>G
ENST00000527700.5:n.3239C>G
ENST00000528725.5:c.373C>G
ENST00000529977.5:n.1578C>G
ENST00000530044.5:c.3646+31C>G	ENSP00000435866.1:n.3646+31C>G
ENST00000531747.1:c.913C>G
ENST00000533737.5:c.340C>G
NM_001243254.1:c.3646+31C>G	NP_001230183.1:n.3646+31C>G
NM_015213.3:c.3677C>G	NP_056028.2:p.Ala1226Gly
XM_005252832.1:c.3677C>G	XP_005252889.1:p.Ala1226Gly
XM_011519952.1:c.3646+31C>G	XP_011518254.1:n.3646+31C>G
XM_011519953.1:c.1775C>G	XP_011518255.1:p.Ala592Gly
XR_242782.2:n.3859C>G
XR_930851.1:n.3828+31C>G
NM_001348749.1:c.3605C>G	NP_001335678.1:p.Ala1202Gly
NM_001348750.1:c.3389C>G	NP_001335679.1:p.Ala1130Gly
NR_145966.2:n.3851C>G
NM_015213.4:c.3677C>G MANE Select	NP_056028.2:p.Ala1226Gly
NM_001243254.2:c.3646+31C>G	NP_001230183.1:n.3646+31C>G
NM_001348749.2:c.3605C>G	NP_001335678.1:p.Ala1202Gly
NM_001348750.2:c.3389C>G	NP_001335679.1:p.Ala1130Gly