Canonical Allele Identifier: CA379597634

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163559G>T (hg19) ; chr11:g.9142012G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142012G>T , CM000673.2:g.9142012G>T	GRCh38
NC_000011.9:g.9163559G>T , CM000673.1:g.9163559G>T	GRCh37
NC_000011.8:g.9120135G>T	NCBI36
NG_053019.1:g.128324C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3608C>A MANE Select	ENSP00000328524.3:p.Thr1203Asn
ENST00000525784.6:n.1470C>A
ENST00000530780.2:c.*3434C>A	ENSP00000433925.1:n.*3434C>A
ENST00000531747.2:n.3279C>A
ENST00000679446.1:n.3529C>A
ENST00000679458.1:n.5009C>A
ENST00000679460.1:n.4670C>A
ENST00000679568.1:c.3608C>A	ENSP00000505860.1:p.Thr1203Asn
ENST00000679745.1:n.4113C>A
ENST00000679773.1:n.2769C>A
ENST00000679926.1:n.4910C>A
ENST00000679999.1:c.*665C>A	ENSP00000505198.1:n.*665C>A
ENST00000680252.1:c.3275C>A
ENST00000680294.1:c.3401C>A	ENSP00000506113.1:p.Thr1134Asn
ENST00000680358.1:n.2907C>A
ENST00000680470.1:c.*1389C>A	ENSP00000505975.1:n.*1389C>A
ENST00000680554.1:c.*141C>A	ENSP00000505621.1:n.*141C>A
ENST00000680576.1:n.5084C>A
ENST00000680599.1:n.3649C>A
ENST00000680742.1:c.*141C>A	ENSP00000505206.1:n.*141C>A
ENST00000680791.1:n.2492C>A
ENST00000680885.1:n.5310C>A
ENST00000681158.1:c.3192C>A
ENST00000681203.1:c.3536C>A	ENSP00000506456.1:p.Thr1179Asn
ENST00000681371.1:n.3480C>A
ENST00000681425.1:n.4086C>A
ENST00000681639.1:n.1887C>A
ENST00000328194.7:c.3608C>A	ENSP00000328524.3:p.Thr1203Asn
ENST00000525784.5:c.544C>A
ENST00000527700.5:n.3170C>A
ENST00000528725.5:c.304C>A
ENST00000529977.5:n.1509C>A
ENST00000530044.5:c.3608C>A	ENSP00000435866.1:p.Thr1203Asn
ENST00000531747.1:c.844C>A
ENST00000533737.5:c.271C>A
NM_001243254.1:c.3608C>A	NP_001230183.1:p.Thr1203Asn
NM_015213.3:c.3608C>A	NP_056028.2:p.Thr1203Asn
XM_005252832.1:c.3608C>A	XP_005252889.1:p.Thr1203Asn
XM_011519952.1:c.3608C>A	XP_011518254.1:p.Thr1203Asn
XM_011519953.1:c.1706C>A	XP_011518255.1:p.Thr569Asn
XR_242782.2:n.3790C>A
XR_930851.1:n.3790C>A
NM_001348749.1:c.3536C>A	NP_001335678.1:p.Thr1179Asn
NM_001348750.1:c.3320C>A	NP_001335679.1:p.Thr1107Asn
NR_145966.2:n.3782C>A
NM_015213.4:c.3608C>A MANE Select	NP_056028.2:p.Thr1203Asn
NM_001243254.2:c.3608C>A	NP_001230183.1:p.Thr1203Asn
NM_001348749.2:c.3536C>A	NP_001335678.1:p.Thr1179Asn
NM_001348750.2:c.3320C>A	NP_001335679.1:p.Thr1107Asn