Canonical Allele Identifier: CA379597815

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9142037-C-T
• MyVariant Identifiers: chr11:g.9163584C>T (hg19) ; chr11:g.9142037C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142037C>T , CM000673.2:g.9142037C>T	GRCh38
NC_000011.9:g.9163584C>T , CM000673.1:g.9163584C>T	GRCh37
NC_000011.8:g.9120160C>T	NCBI36
NG_053019.1:g.128299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3583G>A MANE Select	ENSP00000328524.3:p.Ala1195Thr
ENST00000525784.6:n.1445G>A
ENST00000530780.2:c.*3409G>A	ENSP00000433925.1:n.*3409G>A
ENST00000531747.2:n.3254G>A
ENST00000679446.1:n.3504G>A
ENST00000679458.1:n.4984G>A
ENST00000679460.1:n.4645G>A
ENST00000679568.1:c.3583G>A	ENSP00000505860.1:p.Ala1195Thr
ENST00000679745.1:n.4088G>A
ENST00000679773.1:n.2744G>A
ENST00000679926.1:n.4885G>A
ENST00000679999.1:c.*640G>A	ENSP00000505198.1:n.*640G>A
ENST00000680252.1:c.3250G>A
ENST00000680294.1:c.3376G>A	ENSP00000506113.1:p.Ala1126Thr
ENST00000680358.1:n.2882G>A
ENST00000680470.1:c.*1364G>A	ENSP00000505975.1:n.*1364G>A
ENST00000680554.1:c.*116G>A	ENSP00000505621.1:n.*116G>A
ENST00000680576.1:n.5059G>A
ENST00000680599.1:n.3624G>A
ENST00000680742.1:c.*116G>A	ENSP00000505206.1:n.*116G>A
ENST00000680791.1:n.2467G>A
ENST00000680885.1:n.5285G>A
ENST00000681158.1:c.3167G>A
ENST00000681203.1:c.3511G>A	ENSP00000506456.1:p.Ala1171Thr
ENST00000681371.1:n.3455G>A
ENST00000681425.1:n.4061G>A
ENST00000681639.1:n.1862G>A
ENST00000328194.7:c.3583G>A	ENSP00000328524.3:p.Ala1195Thr
ENST00000525784.5:c.519G>A
ENST00000527700.5:n.3145G>A
ENST00000528725.5:c.279G>A
ENST00000529977.5:n.1484G>A
ENST00000530044.5:c.3583G>A	ENSP00000435866.1:p.Ala1195Thr
ENST00000531747.1:c.819G>A
ENST00000533737.5:c.246G>A
NM_001243254.1:c.3583G>A	NP_001230183.1:p.Ala1195Thr
NM_015213.3:c.3583G>A	NP_056028.2:p.Ala1195Thr
XM_005252832.1:c.3583G>A	XP_005252889.1:p.Ala1195Thr
XM_011519952.1:c.3583G>A	XP_011518254.1:p.Ala1195Thr
XM_011519953.1:c.1681G>A	XP_011518255.1:p.Ala561Thr
XR_242782.2:n.3765G>A
XR_930851.1:n.3765G>A
NM_001348749.1:c.3511G>A	NP_001335678.1:p.Ala1171Thr
NM_001348750.1:c.3295G>A	NP_001335679.1:p.Ala1099Thr
NR_145966.2:n.3757G>A
NM_015213.4:c.3583G>A MANE Select	NP_056028.2:p.Ala1195Thr
NM_001243254.2:c.3583G>A	NP_001230183.1:p.Ala1195Thr
NM_001348749.2:c.3511G>A	NP_001335678.1:p.Ala1171Thr
NM_001348750.2:c.3295G>A	NP_001335679.1:p.Ala1099Thr