Canonical Allele Identifier: CA379597651

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163562A>T (hg19) ; chr11:g.9142015A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142015A>T , CM000673.2:g.9142015A>T	GRCh38
NC_000011.9:g.9163562A>T , CM000673.1:g.9163562A>T	GRCh37
NC_000011.8:g.9120138A>T	NCBI36
NG_053019.1:g.128321T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3605T>A MANE Select	ENSP00000328524.3:p.Val1202Asp
ENST00000525784.6:n.1467T>A
ENST00000530780.2:c.*3431T>A	ENSP00000433925.1:n.*3431T>A
ENST00000531747.2:n.3276T>A
ENST00000679446.1:n.3526T>A
ENST00000679458.1:n.5006T>A
ENST00000679460.1:n.4667T>A
ENST00000679568.1:c.3605T>A	ENSP00000505860.1:p.Val1202Asp
ENST00000679745.1:n.4110T>A
ENST00000679773.1:n.2766T>A
ENST00000679926.1:n.4907T>A
ENST00000679999.1:c.*662T>A	ENSP00000505198.1:n.*662T>A
ENST00000680252.1:c.3272T>A
ENST00000680294.1:c.3398T>A	ENSP00000506113.1:p.Val1133Asp
ENST00000680358.1:n.2904T>A
ENST00000680470.1:c.*1386T>A	ENSP00000505975.1:n.*1386T>A
ENST00000680554.1:c.*138T>A	ENSP00000505621.1:n.*138T>A
ENST00000680576.1:n.5081T>A
ENST00000680599.1:n.3646T>A
ENST00000680742.1:c.*138T>A	ENSP00000505206.1:n.*138T>A
ENST00000680791.1:n.2489T>A
ENST00000680885.1:n.5307T>A
ENST00000681158.1:c.3189T>A
ENST00000681203.1:c.3533T>A	ENSP00000506456.1:p.Val1178Asp
ENST00000681371.1:n.3477T>A
ENST00000681425.1:n.4083T>A
ENST00000681639.1:n.1884T>A
ENST00000328194.7:c.3605T>A	ENSP00000328524.3:p.Val1202Asp
ENST00000525784.5:c.541T>A
ENST00000527700.5:n.3167T>A
ENST00000528725.5:c.301T>A
ENST00000529977.5:n.1506T>A
ENST00000530044.5:c.3605T>A	ENSP00000435866.1:p.Val1202Asp
ENST00000531747.1:c.841T>A
ENST00000533737.5:c.268T>A
NM_001243254.1:c.3605T>A	NP_001230183.1:p.Val1202Asp
NM_015213.3:c.3605T>A	NP_056028.2:p.Val1202Asp
XM_005252832.1:c.3605T>A	XP_005252889.1:p.Val1202Asp
XM_011519952.1:c.3605T>A	XP_011518254.1:p.Val1202Asp
XM_011519953.1:c.1703T>A	XP_011518255.1:p.Val568Asp
XR_242782.2:n.3787T>A
XR_930851.1:n.3787T>A
NM_001348749.1:c.3533T>A	NP_001335678.1:p.Val1178Asp
NM_001348750.1:c.3317T>A	NP_001335679.1:p.Val1106Asp
NR_145966.2:n.3779T>A
NM_015213.4:c.3605T>A MANE Select	NP_056028.2:p.Val1202Asp
NM_001243254.2:c.3605T>A	NP_001230183.1:p.Val1202Asp
NM_001348749.2:c.3533T>A	NP_001335678.1:p.Val1178Asp
NM_001348750.2:c.3317T>A	NP_001335679.1:p.Val1106Asp