Canonical Allele Identifier: CA379597321

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163523T>A (hg19) ; chr11:g.9141976T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141976T>A , CM000673.2:g.9141976T>A	GRCh38
NC_000011.9:g.9163523T>A , CM000673.1:g.9163523T>A	GRCh37
NC_000011.8:g.9120099T>A	NCBI36
NG_053019.1:g.128360A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3644A>T MANE Select	ENSP00000328524.3:p.Asp1215Val
ENST00000525784.6:n.1506A>T
ENST00000530780.2:c.*3470A>T	ENSP00000433925.1:n.*3470A>T
ENST00000531747.2:n.3315A>T
ENST00000679446.1:n.3565A>T
ENST00000679458.1:n.5045A>T
ENST00000679460.1:n.4706A>T
ENST00000679568.1:c.3644A>T	ENSP00000505860.1:p.Asp1215Val
ENST00000679745.1:n.4149A>T
ENST00000679773.1:n.2805A>T
ENST00000679926.1:n.4946A>T
ENST00000679999.1:c.*701A>T	ENSP00000505198.1:n.*701A>T
ENST00000680252.1:c.3311A>T
ENST00000680294.1:c.3437A>T	ENSP00000506113.1:p.Asp1146Val
ENST00000680358.1:n.2943A>T
ENST00000680470.1:c.*1425A>T	ENSP00000505975.1:n.*1425A>T
ENST00000680554.1:c.*177A>T	ENSP00000505621.1:n.*177A>T
ENST00000680576.1:n.5120A>T
ENST00000680599.1:n.3685A>T
ENST00000680742.1:c.*177A>T	ENSP00000505206.1:n.*177A>T
ENST00000680791.1:n.2528A>T
ENST00000680885.1:n.5346A>T
ENST00000681158.1:c.3228A>T
ENST00000681203.1:c.3572A>T	ENSP00000506456.1:p.Asp1191Val
ENST00000681371.1:n.3516A>T
ENST00000681425.1:n.4122A>T
ENST00000681639.1:n.1923A>T
ENST00000328194.7:c.3644A>T	ENSP00000328524.3:p.Asp1215Val
ENST00000525784.5:c.580A>T
ENST00000527700.5:n.3206A>T
ENST00000528725.5:c.340A>T
ENST00000529977.5:n.1545A>T
ENST00000530044.5:c.3644A>T	ENSP00000435866.1:p.Asp1215Val
ENST00000531747.1:c.880A>T
ENST00000533737.5:c.307A>T
NM_001243254.1:c.3644A>T	NP_001230183.1:p.Asp1215Val
NM_015213.3:c.3644A>T	NP_056028.2:p.Asp1215Val
XM_005252832.1:c.3644A>T	XP_005252889.1:p.Asp1215Val
XM_011519952.1:c.3644A>T	XP_011518254.1:p.Asp1215Val
XM_011519953.1:c.1742A>T	XP_011518255.1:p.Asp581Val
XR_242782.2:n.3826A>T
XR_930851.1:n.3826A>T
NM_001348749.1:c.3572A>T	NP_001335678.1:p.Asp1191Val
NM_001348750.1:c.3356A>T	NP_001335679.1:p.Asp1119Val
NR_145966.2:n.3818A>T
NM_015213.4:c.3644A>T MANE Select	NP_056028.2:p.Asp1215Val
NM_001243254.2:c.3644A>T	NP_001230183.1:p.Asp1215Val
NM_001348749.2:c.3572A>T	NP_001335678.1:p.Asp1191Val
NM_001348750.2:c.3356A>T	NP_001335679.1:p.Asp1119Val