Canonical Allele Identifier: CA379597559

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163546A>C (hg19) ; chr11:g.9141999A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141999A>C , CM000673.2:g.9141999A>C	GRCh38
NC_000011.9:g.9163546A>C , CM000673.1:g.9163546A>C	GRCh37
NC_000011.8:g.9120122A>C	NCBI36
NG_053019.1:g.128337T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3621T>G MANE Select	ENSP00000328524.3:p.Asn1207Lys
ENST00000525784.6:n.1483T>G
ENST00000530780.2:c.*3447T>G	ENSP00000433925.1:n.*3447T>G
ENST00000531747.2:n.3292T>G
ENST00000679446.1:n.3542T>G
ENST00000679458.1:n.5022T>G
ENST00000679460.1:n.4683T>G
ENST00000679568.1:c.3621T>G	ENSP00000505860.1:p.Asn1207Lys
ENST00000679745.1:n.4126T>G
ENST00000679773.1:n.2782T>G
ENST00000679926.1:n.4923T>G
ENST00000679999.1:c.*678T>G	ENSP00000505198.1:n.*678T>G
ENST00000680252.1:c.3288T>G
ENST00000680294.1:c.3414T>G	ENSP00000506113.1:p.Asn1138Lys
ENST00000680358.1:n.2920T>G
ENST00000680470.1:c.*1402T>G	ENSP00000505975.1:n.*1402T>G
ENST00000680554.1:c.*154T>G	ENSP00000505621.1:n.*154T>G
ENST00000680576.1:n.5097T>G
ENST00000680599.1:n.3662T>G
ENST00000680742.1:c.*154T>G	ENSP00000505206.1:n.*154T>G
ENST00000680791.1:n.2505T>G
ENST00000680885.1:n.5323T>G
ENST00000681158.1:c.3205T>G
ENST00000681203.1:c.3549T>G	ENSP00000506456.1:p.Asn1183Lys
ENST00000681371.1:n.3493T>G
ENST00000681425.1:n.4099T>G
ENST00000681639.1:n.1900T>G
ENST00000328194.7:c.3621T>G	ENSP00000328524.3:p.Asn1207Lys
ENST00000525784.5:c.557T>G
ENST00000527700.5:n.3183T>G
ENST00000528725.5:c.317T>G
ENST00000529977.5:n.1522T>G
ENST00000530044.5:c.3621T>G	ENSP00000435866.1:p.Asn1207Lys
ENST00000531747.1:c.857T>G
ENST00000533737.5:c.284T>G
NM_001243254.1:c.3621T>G	NP_001230183.1:p.Asn1207Lys
NM_015213.3:c.3621T>G	NP_056028.2:p.Asn1207Lys
XM_005252832.1:c.3621T>G	XP_005252889.1:p.Asn1207Lys
XM_011519952.1:c.3621T>G	XP_011518254.1:p.Asn1207Lys
XM_011519953.1:c.1719T>G	XP_011518255.1:p.Asn573Lys
XR_242782.2:n.3803T>G
XR_930851.1:n.3803T>G
NM_001348749.1:c.3549T>G	NP_001335678.1:p.Asn1183Lys
NM_001348750.1:c.3333T>G	NP_001335679.1:p.Asn1111Lys
NR_145966.2:n.3795T>G
NM_015213.4:c.3621T>G MANE Select	NP_056028.2:p.Asn1207Lys
NM_001243254.2:c.3621T>G	NP_001230183.1:p.Asn1207Lys
NM_001348749.2:c.3549T>G	NP_001335678.1:p.Asn1183Lys
NM_001348750.2:c.3333T>G	NP_001335679.1:p.Asn1111Lys