Canonical Allele Identifier: CA473040266

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163630T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142083T>G , CM000673.2:g.9142083T>G	GRCh38
NC_000011.9:g.9163630T>G , CM000673.1:g.9163630T>G	GRCh37
NC_000011.8:g.9120206T>G	NCBI36
NG_053019.1:g.128253A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3537A>C MANE Select	ENSP00000328524.3:p.Thr1179=
ENST00000525784.6:n.1399A>C
ENST00000530780.2:c.*3363A>C	ENSP00000433925.1:n.*3363A>C
ENST00000531747.2:n.3208A>C
ENST00000679446.1:n.3458A>C
ENST00000679458.1:n.4938A>C
ENST00000679460.1:n.4599A>C
ENST00000679568.1:c.3537A>C	ENSP00000505860.1:p.Thr1179=
ENST00000679745.1:n.4042A>C
ENST00000679773.1:n.2698A>C
ENST00000679926.1:n.4839A>C
ENST00000679999.1:c.*594A>C	ENSP00000505198.1:n.*594A>C
ENST00000680252.1:c.3204A>C
ENST00000680294.1:c.3330A>C	ENSP00000506113.1:p.Thr1110=
ENST00000680358.1:n.2836A>C
ENST00000680470.1:c.*1318A>C	ENSP00000505975.1:n.*1318A>C
ENST00000680554.1:c.*70A>C	ENSP00000505621.1:n.*70A>C
ENST00000680576.1:n.5013A>C
ENST00000680599.1:n.3578A>C
ENST00000680742.1:c.*70A>C	ENSP00000505206.1:n.*70A>C
ENST00000680791.1:n.2421A>C
ENST00000680885.1:n.5239A>C
ENST00000681158.1:c.3121A>C
ENST00000681203.1:c.3465A>C	ENSP00000506456.1:p.Thr1155=
ENST00000681371.1:n.3409A>C
ENST00000681425.1:n.4015A>C
ENST00000681639.1:n.1816A>C
ENST00000328194.7:c.3537A>C	ENSP00000328524.3:p.Thr1179=
ENST00000525784.5:c.473A>C
ENST00000527700.5:n.3099A>C
ENST00000528725.5:c.233A>C
ENST00000529977.5:n.1438A>C
ENST00000530044.5:c.3537A>C	ENSP00000435866.1:p.Thr1179=
ENST00000531747.1:c.773A>C
ENST00000533737.5:c.200A>C
NM_001243254.1:c.3537A>C	NP_001230183.1:p.Thr1179=
NM_015213.3:c.3537A>C	NP_056028.2:p.Thr1179=
XM_005252832.1:c.3537A>C	XP_005252889.1:p.Thr1179=
XM_011519952.1:c.3537A>C	XP_011518254.1:p.Thr1179=
XM_011519953.1:c.1635A>C	XP_011518255.1:p.Thr545=
XR_242782.2:n.3719A>C
XR_930851.1:n.3719A>C
NM_001348749.1:c.3465A>C	NP_001335678.1:p.Thr1155=
NM_001348750.1:c.3249A>C	NP_001335679.1:p.Thr1083=
NR_145966.2:n.3711A>C
NM_015213.4:c.3537A>C MANE Select	NP_056028.2:p.Thr1179=
NM_001243254.2:c.3537A>C	NP_001230183.1:p.Thr1179=
NM_001348749.2:c.3465A>C	NP_001335678.1:p.Thr1155=
NM_001348750.2:c.3249A>C	NP_001335679.1:p.Thr1083=