Canonical Allele Identifier: CA473040269

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163639A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142092A>G , CM000673.2:g.9142092A>G	GRCh38
NC_000011.9:g.9163639A>G , CM000673.1:g.9163639A>G	GRCh37
NC_000011.8:g.9120215A>G	NCBI36
NG_053019.1:g.128244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3528T>C MANE Select	ENSP00000328524.3:p.Tyr1176=
ENST00000525784.6:n.1390T>C
ENST00000530780.2:c.*3354T>C	ENSP00000433925.1:n.*3354T>C
ENST00000531747.2:n.3199T>C
ENST00000679446.1:n.3449T>C
ENST00000679458.1:n.4929T>C
ENST00000679460.1:n.4590T>C
ENST00000679568.1:c.3528T>C	ENSP00000505860.1:p.Tyr1176=
ENST00000679745.1:n.4033T>C
ENST00000679773.1:n.2689T>C
ENST00000679926.1:n.4830T>C
ENST00000679999.1:c.*585T>C	ENSP00000505198.1:n.*585T>C
ENST00000680252.1:c.3195T>C
ENST00000680294.1:c.3321T>C	ENSP00000506113.1:p.Tyr1107=
ENST00000680358.1:n.2827T>C
ENST00000680470.1:c.*1309T>C	ENSP00000505975.1:n.*1309T>C
ENST00000680554.1:c.*61T>C	ENSP00000505621.1:n.*61T>C
ENST00000680576.1:n.5004T>C
ENST00000680599.1:n.3569T>C
ENST00000680742.1:c.*61T>C	ENSP00000505206.1:n.*61T>C
ENST00000680791.1:n.2412T>C
ENST00000680885.1:n.5230T>C
ENST00000681158.1:c.3112T>C
ENST00000681203.1:c.3456T>C	ENSP00000506456.1:p.Tyr1152=
ENST00000681371.1:n.3400T>C
ENST00000681425.1:n.4006T>C
ENST00000681639.1:n.1807T>C
ENST00000328194.7:c.3528T>C	ENSP00000328524.3:p.Tyr1176=
ENST00000525784.5:c.464T>C
ENST00000527700.5:n.3090T>C
ENST00000528725.5:c.224T>C
ENST00000529977.5:n.1429T>C
ENST00000530044.5:c.3528T>C	ENSP00000435866.1:p.Tyr1176=
ENST00000531747.1:c.764T>C
ENST00000533737.5:c.191T>C
NM_001243254.1:c.3528T>C	NP_001230183.1:p.Tyr1176=
NM_015213.3:c.3528T>C	NP_056028.2:p.Tyr1176=
XM_005252832.1:c.3528T>C	XP_005252889.1:p.Tyr1176=
XM_011519952.1:c.3528T>C	XP_011518254.1:p.Tyr1176=
XM_011519953.1:c.1626T>C	XP_011518255.1:p.Tyr542=
XR_242782.2:n.3710T>C
XR_930851.1:n.3710T>C
NM_001348749.1:c.3456T>C	NP_001335678.1:p.Tyr1152=
NM_001348750.1:c.3240T>C	NP_001335679.1:p.Tyr1080=
NR_145966.2:n.3702T>C
NM_015213.4:c.3528T>C MANE Select	NP_056028.2:p.Tyr1176=
NM_001243254.2:c.3528T>C	NP_001230183.1:p.Tyr1176=
NM_001348749.2:c.3456T>C	NP_001335678.1:p.Tyr1152=
NM_001348750.2:c.3240T>C	NP_001335679.1:p.Tyr1080=