Canonical Allele Identifier: CA379608480

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182376C>G (hg19) ; chr11:g.9160829C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160829C>G , CM000673.2:g.9160829C>G	GRCh38
NC_000011.9:g.9182376C>G , CM000673.1:g.9182376C>G	GRCh37
NC_000011.8:g.9138952C>G	NCBI36
NG_053019.1:g.109507G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2320G>C MANE Select	ENSP00000328524.3:p.Ala774Pro
ENST00000530780.2:c.*2146G>C	ENSP00000433925.1:n.*2146G>C
ENST00000679446.1:n.2241G>C
ENST00000679458.1:n.3721G>C
ENST00000679460.1:n.2109G>C
ENST00000679568.1:c.2320G>C	ENSP00000505860.1:p.Ala774Pro
ENST00000679745.1:n.2109G>C
ENST00000679926.1:n.1136G>C
ENST00000679999.1:c.2320G>C	ENSP00000505198.1:p.Ala774Pro
ENST00000680252.1:c.2109G>C
ENST00000680294.1:c.2320G>C	ENSP00000506113.1:p.Ala774Pro
ENST00000680358.1:n.1619G>C
ENST00000680470.1:c.*186G>C	ENSP00000505975.1:n.*186G>C
ENST00000680554.1:c.2032G>C	ENSP00000505621.1:p.Ala678Pro
ENST00000680576.1:n.2109G>C
ENST00000680599.1:n.2237G>C
ENST00000680742.1:c.2320G>C	ENSP00000505206.1:p.Ala774Pro
ENST00000680885.1:n.2241G>C
ENST00000681158.1:c.2109G>C
ENST00000681173.1:n.2109G>C
ENST00000681203.1:c.2248G>C	ENSP00000506456.1:p.Ala750Pro
ENST00000681425.1:n.2241G>C
ENST00000328194.7:c.2320G>C	ENSP00000328524.3:p.Ala774Pro
ENST00000526707.5:c.2248G>C	ENSP00000436780.1:p.Ala750Pro
ENST00000527700.5:n.1882G>C
ENST00000530044.5:c.2320G>C	ENSP00000435866.1:p.Ala774Pro
NM_001243254.1:c.2320G>C	NP_001230183.1:p.Ala774Pro
NM_015213.3:c.2320G>C	NP_056028.2:p.Ala774Pro
XM_005252832.1:c.2320G>C	XP_005252889.1:p.Ala774Pro
XM_011519952.1:c.2320G>C	XP_011518254.1:p.Ala774Pro
XM_011519953.1:c.418G>C	XP_011518255.1:p.Ala140Pro
XR_242782.2:n.2585G>C
XR_930851.1:n.2585G>C
XR_930852.1:n.2585G>C
XR_930853.1:n.2434G>C
NM_001348749.1:c.2248G>C	NP_001335678.1:p.Ala750Pro
NM_001348750.1:c.2032G>C	NP_001335679.1:p.Ala678Pro
NR_145966.2:n.2577G>C
NM_015213.4:c.2320G>C MANE Select	NP_056028.2:p.Ala774Pro
NM_001243254.2:c.2320G>C	NP_001230183.1:p.Ala774Pro
NM_001348749.2:c.2248G>C	NP_001335678.1:p.Ala750Pro
NM_001348750.2:c.2032G>C	NP_001335679.1:p.Ala678Pro