Canonical Allele Identifier: CA379598230

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163645T>G (hg19) ; chr11:g.9142098T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142098T>G , CM000673.2:g.9142098T>G	GRCh38
NC_000011.9:g.9163645T>G , CM000673.1:g.9163645T>G	GRCh37
NC_000011.8:g.9120221T>G	NCBI36
NG_053019.1:g.128238A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3522A>C MANE Select	ENSP00000328524.3:p.Gln1174His
ENST00000525784.6:n.1384A>C
ENST00000530780.2:c.*3348A>C	ENSP00000433925.1:n.*3348A>C
ENST00000531747.2:n.3193A>C
ENST00000679446.1:n.3443A>C
ENST00000679458.1:n.4923A>C
ENST00000679460.1:n.4584A>C
ENST00000679568.1:c.3522A>C	ENSP00000505860.1:p.Gln1174His
ENST00000679745.1:n.4027A>C
ENST00000679773.1:n.2683A>C
ENST00000679926.1:n.4824A>C
ENST00000679999.1:c.*579A>C	ENSP00000505198.1:n.*579A>C
ENST00000680252.1:c.3189A>C
ENST00000680294.1:c.3315A>C	ENSP00000506113.1:p.Gln1105His
ENST00000680358.1:n.2821A>C
ENST00000680470.1:c.*1303A>C	ENSP00000505975.1:n.*1303A>C
ENST00000680554.1:c.*55A>C	ENSP00000505621.1:n.*55A>C
ENST00000680576.1:n.4998A>C
ENST00000680599.1:n.3563A>C
ENST00000680742.1:c.*55A>C	ENSP00000505206.1:n.*55A>C
ENST00000680791.1:n.2406A>C
ENST00000680885.1:n.5224A>C
ENST00000681158.1:c.3106A>C
ENST00000681203.1:c.3450A>C	ENSP00000506456.1:p.Gln1150His
ENST00000681371.1:n.3394A>C
ENST00000681425.1:n.4000A>C
ENST00000681639.1:n.1801A>C
ENST00000328194.7:c.3522A>C	ENSP00000328524.3:p.Gln1174His
ENST00000525784.5:c.458A>C
ENST00000527700.5:n.3084A>C
ENST00000528725.5:c.218A>C
ENST00000529977.5:n.1423A>C
ENST00000530044.5:c.3522A>C	ENSP00000435866.1:p.Gln1174His
ENST00000531747.1:c.758A>C
ENST00000533737.5:c.185A>C
NM_001243254.1:c.3522A>C	NP_001230183.1:p.Gln1174His
NM_015213.3:c.3522A>C	NP_056028.2:p.Gln1174His
XM_005252832.1:c.3522A>C	XP_005252889.1:p.Gln1174His
XM_011519952.1:c.3522A>C	XP_011518254.1:p.Gln1174His
XM_011519953.1:c.1620A>C	XP_011518255.1:p.Gln540His
XR_242782.2:n.3704A>C
XR_930851.1:n.3704A>C
NM_001348749.1:c.3450A>C	NP_001335678.1:p.Gln1150His
NM_001348750.1:c.3234A>C	NP_001335679.1:p.Gln1078His
NR_145966.2:n.3696A>C
NM_015213.4:c.3522A>C MANE Select	NP_056028.2:p.Gln1174His
NM_001243254.2:c.3522A>C	NP_001230183.1:p.Gln1174His
NM_001348749.2:c.3450A>C	NP_001335678.1:p.Gln1150His
NM_001348750.2:c.3234A>C	NP_001335679.1:p.Gln1078His