Canonical Allele Identifier: CA379597754

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163576G>T (hg19) ; chr11:g.9142029G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142029G>T , CM000673.2:g.9142029G>T	GRCh38
NC_000011.9:g.9163576G>T , CM000673.1:g.9163576G>T	GRCh37
NC_000011.8:g.9120152G>T	NCBI36
NG_053019.1:g.128307C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3591C>A MANE Select	ENSP00000328524.3:p.Asn1197Lys
ENST00000525784.6:n.1453C>A
ENST00000530780.2:c.*3417C>A	ENSP00000433925.1:n.*3417C>A
ENST00000531747.2:n.3262C>A
ENST00000679446.1:n.3512C>A
ENST00000679458.1:n.4992C>A
ENST00000679460.1:n.4653C>A
ENST00000679568.1:c.3591C>A	ENSP00000505860.1:p.Asn1197Lys
ENST00000679745.1:n.4096C>A
ENST00000679773.1:n.2752C>A
ENST00000679926.1:n.4893C>A
ENST00000679999.1:c.*648C>A	ENSP00000505198.1:n.*648C>A
ENST00000680252.1:c.3258C>A
ENST00000680294.1:c.3384C>A	ENSP00000506113.1:p.Asn1128Lys
ENST00000680358.1:n.2890C>A
ENST00000680470.1:c.*1372C>A	ENSP00000505975.1:n.*1372C>A
ENST00000680554.1:c.*124C>A	ENSP00000505621.1:n.*124C>A
ENST00000680576.1:n.5067C>A
ENST00000680599.1:n.3632C>A
ENST00000680742.1:c.*124C>A	ENSP00000505206.1:n.*124C>A
ENST00000680791.1:n.2475C>A
ENST00000680885.1:n.5293C>A
ENST00000681158.1:c.3175C>A
ENST00000681203.1:c.3519C>A	ENSP00000506456.1:p.Asn1173Lys
ENST00000681371.1:n.3463C>A
ENST00000681425.1:n.4069C>A
ENST00000681639.1:n.1870C>A
ENST00000328194.7:c.3591C>A	ENSP00000328524.3:p.Asn1197Lys
ENST00000525784.5:c.527C>A
ENST00000527700.5:n.3153C>A
ENST00000528725.5:c.287C>A
ENST00000529977.5:n.1492C>A
ENST00000530044.5:c.3591C>A	ENSP00000435866.1:p.Asn1197Lys
ENST00000531747.1:c.827C>A
ENST00000533737.5:c.254C>A
NM_001243254.1:c.3591C>A	NP_001230183.1:p.Asn1197Lys
NM_015213.3:c.3591C>A	NP_056028.2:p.Asn1197Lys
XM_005252832.1:c.3591C>A	XP_005252889.1:p.Asn1197Lys
XM_011519952.1:c.3591C>A	XP_011518254.1:p.Asn1197Lys
XM_011519953.1:c.1689C>A	XP_011518255.1:p.Asn563Lys
XR_242782.2:n.3773C>A
XR_930851.1:n.3773C>A
NM_001348749.1:c.3519C>A	NP_001335678.1:p.Asn1173Lys
NM_001348750.1:c.3303C>A	NP_001335679.1:p.Asn1101Lys
NR_145966.2:n.3765C>A
NM_015213.4:c.3591C>A MANE Select	NP_056028.2:p.Asn1197Lys
NM_001243254.2:c.3591C>A	NP_001230183.1:p.Asn1197Lys
NM_001348749.2:c.3519C>A	NP_001335678.1:p.Asn1173Lys
NM_001348750.2:c.3303C>A	NP_001335679.1:p.Asn1101Lys