Canonical Allele Identifier: CA379597180

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163503C>T (hg19) ; chr11:g.9141956C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141956C>T , CM000673.2:g.9141956C>T	GRCh38
NC_000011.9:g.9163503C>T , CM000673.1:g.9163503C>T	GRCh37
NC_000011.8:g.9120079C>T	NCBI36
NG_053019.1:g.128380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3664G>A MANE Select	ENSP00000328524.3:p.Val1222Met
ENST00000525784.6:n.1526G>A
ENST00000530780.2:c.*3490G>A	ENSP00000433925.1:n.*3490G>A
ENST00000531747.2:n.3335G>A
ENST00000679446.1:n.3585G>A
ENST00000679458.1:n.5065G>A
ENST00000679460.1:n.4726G>A
ENST00000679568.1:c.3664G>A	ENSP00000505860.1:p.Val1222Met
ENST00000679745.1:n.4169G>A
ENST00000679773.1:n.2825G>A
ENST00000679926.1:n.4966G>A
ENST00000679999.1:c.*721G>A	ENSP00000505198.1:n.*721G>A
ENST00000680252.1:c.3331G>A
ENST00000680294.1:c.3457G>A	ENSP00000506113.1:p.Val1153Met
ENST00000680358.1:n.2963G>A
ENST00000680470.1:c.*1445G>A	ENSP00000505975.1:n.*1445G>A
ENST00000680554.1:c.*197G>A	ENSP00000505621.1:n.*197G>A
ENST00000680576.1:n.5140G>A
ENST00000680599.1:n.3705G>A
ENST00000680742.1:c.*179+18G>A	ENSP00000505206.1:n.*179+18G>A
ENST00000680791.1:n.2548G>A
ENST00000680885.1:n.5366G>A
ENST00000681158.1:c.3248G>A
ENST00000681203.1:c.3592G>A	ENSP00000506456.1:p.Val1198Met
ENST00000681371.1:n.3536G>A
ENST00000681425.1:n.4142G>A
ENST00000681639.1:n.1943G>A
ENST00000328194.7:c.3664G>A	ENSP00000328524.3:p.Val1222Met
ENST00000525784.5:c.600G>A
ENST00000527700.5:n.3226G>A
ENST00000528725.5:c.360G>A
ENST00000529977.5:n.1565G>A
ENST00000530044.5:c.3646+18G>A	ENSP00000435866.1:n.3646+18G>A
ENST00000531747.1:c.900G>A
ENST00000533737.5:c.327G>A
NM_001243254.1:c.3646+18G>A	NP_001230183.1:n.3646+18G>A
NM_015213.3:c.3664G>A	NP_056028.2:p.Val1222Met
XM_005252832.1:c.3664G>A	XP_005252889.1:p.Val1222Met
XM_011519952.1:c.3646+18G>A	XP_011518254.1:n.3646+18G>A
XM_011519953.1:c.1762G>A	XP_011518255.1:p.Val588Met
XR_242782.2:n.3846G>A
XR_930851.1:n.3828+18G>A
NM_001348749.1:c.3592G>A	NP_001335678.1:p.Val1198Met
NM_001348750.1:c.3376G>A	NP_001335679.1:p.Val1126Met
NR_145966.2:n.3838G>A
NM_015213.4:c.3664G>A MANE Select	NP_056028.2:p.Val1222Met
NM_001243254.2:c.3646+18G>A	NP_001230183.1:n.3646+18G>A
NM_001348749.2:c.3592G>A	NP_001335678.1:p.Val1198Met
NM_001348750.2:c.3376G>A	NP_001335679.1:p.Val1126Met