Canonical Allele Identifier: CA473044192

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182341T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160794T>G , CM000673.2:g.9160794T>G	GRCh38
NC_000011.9:g.9182341T>G , CM000673.1:g.9182341T>G	GRCh37
NC_000011.8:g.9138917T>G	NCBI36
NG_053019.1:g.109542A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2355A>C MANE Select	ENSP00000328524.3:p.Thr785=
ENST00000530780.2:c.*2181A>C	ENSP00000433925.1:n.*2181A>C
ENST00000679446.1:n.2276A>C
ENST00000679458.1:n.3756A>C
ENST00000679460.1:n.2144A>C
ENST00000679568.1:c.2355A>C	ENSP00000505860.1:p.Thr785=
ENST00000679745.1:n.2144A>C
ENST00000679926.1:n.1171A>C
ENST00000679999.1:c.2355A>C	ENSP00000505198.1:p.Thr785=
ENST00000680252.1:c.2144A>C
ENST00000680294.1:c.2355A>C	ENSP00000506113.1:p.Thr785=
ENST00000680358.1:n.1654A>C
ENST00000680470.1:c.*221A>C	ENSP00000505975.1:n.*221A>C
ENST00000680554.1:c.2067A>C	ENSP00000505621.1:p.Thr689=
ENST00000680576.1:n.2144A>C
ENST00000680599.1:n.2272A>C
ENST00000680742.1:c.2355A>C	ENSP00000505206.1:p.Thr785=
ENST00000680885.1:n.2276A>C
ENST00000681158.1:c.2144A>C
ENST00000681173.1:n.2144A>C
ENST00000681203.1:c.2283A>C	ENSP00000506456.1:p.Thr761=
ENST00000681425.1:n.2276A>C
ENST00000328194.7:c.2355A>C	ENSP00000328524.3:p.Thr785=
ENST00000526707.5:c.2283A>C	ENSP00000436780.1:p.Thr761=
ENST00000527700.5:n.1917A>C
ENST00000530044.5:c.2355A>C	ENSP00000435866.1:p.Thr785=
NM_001243254.1:c.2355A>C	NP_001230183.1:p.Thr785=
NM_015213.3:c.2355A>C	NP_056028.2:p.Thr785=
XM_005252832.1:c.2355A>C	XP_005252889.1:p.Thr785=
XM_011519952.1:c.2355A>C	XP_011518254.1:p.Thr785=
XM_011519953.1:c.453A>C	XP_011518255.1:p.Thr151=
XR_242782.2:n.2620A>C
XR_930851.1:n.2620A>C
XR_930852.1:n.2620A>C
XR_930853.1:n.2469A>C
NM_001348749.1:c.2283A>C	NP_001335678.1:p.Thr761=
NM_001348750.1:c.2067A>C	NP_001335679.1:p.Thr689=
NR_145966.2:n.2612A>C
NM_015213.4:c.2355A>C MANE Select	NP_056028.2:p.Thr785=
NM_001243254.2:c.2355A>C	NP_001230183.1:p.Thr785=
NM_001348749.2:c.2283A>C	NP_001335678.1:p.Thr761=
NM_001348750.2:c.2067A>C	NP_001335679.1:p.Thr689=