Canonical Allele Identifier: CA379597758

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163577T>C (hg19) ; chr11:g.9142030T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142030T>C , CM000673.2:g.9142030T>C	GRCh38
NC_000011.9:g.9163577T>C , CM000673.1:g.9163577T>C	GRCh37
NC_000011.8:g.9120153T>C	NCBI36
NG_053019.1:g.128306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3590A>G MANE Select	ENSP00000328524.3:p.Asn1197Ser
ENST00000525784.6:n.1452A>G
ENST00000530780.2:c.*3416A>G	ENSP00000433925.1:n.*3416A>G
ENST00000531747.2:n.3261A>G
ENST00000679446.1:n.3511A>G
ENST00000679458.1:n.4991A>G
ENST00000679460.1:n.4652A>G
ENST00000679568.1:c.3590A>G	ENSP00000505860.1:p.Asn1197Ser
ENST00000679745.1:n.4095A>G
ENST00000679773.1:n.2751A>G
ENST00000679926.1:n.4892A>G
ENST00000679999.1:c.*647A>G	ENSP00000505198.1:n.*647A>G
ENST00000680252.1:c.3257A>G
ENST00000680294.1:c.3383A>G	ENSP00000506113.1:p.Asn1128Ser
ENST00000680358.1:n.2889A>G
ENST00000680470.1:c.*1371A>G	ENSP00000505975.1:n.*1371A>G
ENST00000680554.1:c.*123A>G	ENSP00000505621.1:n.*123A>G
ENST00000680576.1:n.5066A>G
ENST00000680599.1:n.3631A>G
ENST00000680742.1:c.*123A>G	ENSP00000505206.1:n.*123A>G
ENST00000680791.1:n.2474A>G
ENST00000680885.1:n.5292A>G
ENST00000681158.1:c.3174A>G
ENST00000681203.1:c.3518A>G	ENSP00000506456.1:p.Asn1173Ser
ENST00000681371.1:n.3462A>G
ENST00000681425.1:n.4068A>G
ENST00000681639.1:n.1869A>G
ENST00000328194.7:c.3590A>G	ENSP00000328524.3:p.Asn1197Ser
ENST00000525784.5:c.526A>G
ENST00000527700.5:n.3152A>G
ENST00000528725.5:c.286A>G
ENST00000529977.5:n.1491A>G
ENST00000530044.5:c.3590A>G	ENSP00000435866.1:p.Asn1197Ser
ENST00000531747.1:c.826A>G
ENST00000533737.5:c.253A>G
NM_001243254.1:c.3590A>G	NP_001230183.1:p.Asn1197Ser
NM_015213.3:c.3590A>G	NP_056028.2:p.Asn1197Ser
XM_005252832.1:c.3590A>G	XP_005252889.1:p.Asn1197Ser
XM_011519952.1:c.3590A>G	XP_011518254.1:p.Asn1197Ser
XM_011519953.1:c.1688A>G	XP_011518255.1:p.Asn563Ser
XR_242782.2:n.3772A>G
XR_930851.1:n.3772A>G
NM_001348749.1:c.3518A>G	NP_001335678.1:p.Asn1173Ser
NM_001348750.1:c.3302A>G	NP_001335679.1:p.Asn1101Ser
NR_145966.2:n.3764A>G
NM_015213.4:c.3590A>G MANE Select	NP_056028.2:p.Asn1197Ser
NM_001243254.2:c.3590A>G	NP_001230183.1:p.Asn1197Ser
NM_001348749.2:c.3518A>G	NP_001335678.1:p.Asn1173Ser
NM_001348750.2:c.3302A>G	NP_001335679.1:p.Asn1101Ser