Canonical Allele Identifier: CA379598197

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163639A>C (hg19) ; chr11:g.9142092A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3528T>G MANE Select	ENSP00000328524.3:p.Tyr1176Ter
ENST00000525784.6:n.1390T>G
ENST00000530780.2:c.*3354T>G	ENSP00000433925.1:n.*3354T>G
ENST00000531747.2:n.3199T>G
ENST00000679446.1:n.3449T>G
ENST00000679458.1:n.4929T>G
ENST00000679460.1:n.4590T>G
ENST00000679568.1:c.3528T>G	ENSP00000505860.1:p.Tyr1176Ter
ENST00000679745.1:n.4033T>G
ENST00000679773.1:n.2689T>G
ENST00000679926.1:n.4830T>G
ENST00000679999.1:c.*585T>G	ENSP00000505198.1:n.*585T>G
ENST00000680252.1:c.3195T>G
ENST00000680294.1:c.3321T>G	ENSP00000506113.1:p.Tyr1107Ter
ENST00000680358.1:n.2827T>G
ENST00000680470.1:c.*1309T>G	ENSP00000505975.1:n.*1309T>G
ENST00000680554.1:c.*61T>G	ENSP00000505621.1:n.*61T>G
ENST00000680576.1:n.5004T>G
ENST00000680599.1:n.3569T>G
ENST00000680742.1:c.*61T>G	ENSP00000505206.1:n.*61T>G
ENST00000680791.1:n.2412T>G
ENST00000680885.1:n.5230T>G
ENST00000681158.1:c.3112T>G
ENST00000681203.1:c.3456T>G	ENSP00000506456.1:p.Tyr1152Ter
ENST00000681371.1:n.3400T>G
ENST00000681425.1:n.4006T>G
ENST00000681639.1:n.1807T>G
ENST00000328194.7:c.3528T>G	ENSP00000328524.3:p.Tyr1176Ter
ENST00000525784.5:c.464T>G
ENST00000527700.5:n.3090T>G
ENST00000528725.5:c.224T>G
ENST00000529977.5:n.1429T>G
ENST00000530044.5:c.3528T>G	ENSP00000435866.1:p.Tyr1176Ter
ENST00000531747.1:c.764T>G
ENST00000533737.5:c.191T>G
NM_001243254.1:c.3528T>G	NP_001230183.1:p.Tyr1176Ter
NM_015213.3:c.3528T>G	NP_056028.2:p.Tyr1176Ter
XM_005252832.1:c.3528T>G	XP_005252889.1:p.Tyr1176Ter
XM_011519952.1:c.3528T>G	XP_011518254.1:p.Tyr1176Ter
XM_011519953.1:c.1626T>G	XP_011518255.1:p.Tyr542Ter
XR_242782.2:n.3710T>G
XR_930851.1:n.3710T>G
NM_001348749.1:c.3456T>G	NP_001335678.1:p.Tyr1152Ter
NM_001348750.1:c.3240T>G	NP_001335679.1:p.Tyr1080Ter
NR_145966.2:n.3702T>G
NM_015213.4:c.3528T>G MANE Select	NP_056028.2:p.Tyr1176Ter
NM_001243254.2:c.3528T>G	NP_001230183.1:p.Tyr1176Ter
NM_001348749.2:c.3456T>G	NP_001335678.1:p.Tyr1152Ter
NM_001348750.2:c.3240T>G	NP_001335679.1:p.Tyr1080Ter