Canonical Allele Identifier: CA379607789

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182286A>C (hg19) ; chr11:g.9160739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160739A>C , CM000673.2:g.9160739A>C	GRCh38
NC_000011.9:g.9182286A>C , CM000673.1:g.9182286A>C	GRCh37
NC_000011.8:g.9138862A>C	NCBI36
NG_053019.1:g.109597T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2410T>G MANE Select	ENSP00000328524.3:p.Trp804Gly
ENST00000530780.2:c.*2236T>G	ENSP00000433925.1:n.*2236T>G
ENST00000679446.1:n.2331T>G
ENST00000679458.1:n.3811T>G
ENST00000679460.1:n.2199T>G
ENST00000679568.1:c.2410T>G	ENSP00000505860.1:p.Trp804Gly
ENST00000679745.1:n.2199T>G
ENST00000679926.1:n.1226T>G
ENST00000679999.1:c.2410T>G	ENSP00000505198.1:p.Trp804Gly
ENST00000680252.1:c.2199T>G
ENST00000680294.1:c.2410T>G	ENSP00000506113.1:p.Trp804Gly
ENST00000680358.1:n.1709T>G
ENST00000680470.1:c.*276T>G	ENSP00000505975.1:n.*276T>G
ENST00000680554.1:c.2122T>G	ENSP00000505621.1:p.Trp708Gly
ENST00000680576.1:n.2199T>G
ENST00000680599.1:n.2327T>G
ENST00000680742.1:c.2410T>G	ENSP00000505206.1:p.Trp804Gly
ENST00000680885.1:n.2331T>G
ENST00000681158.1:c.2199T>G
ENST00000681173.1:n.2199T>G
ENST00000681203.1:c.2338T>G	ENSP00000506456.1:p.Trp780Gly
ENST00000681425.1:n.2331T>G
ENST00000328194.7:c.2410T>G	ENSP00000328524.3:p.Trp804Gly
ENST00000526707.5:c.2338T>G	ENSP00000436780.1:p.Trp780Gly
ENST00000527700.5:n.1972T>G
ENST00000530044.5:c.2410T>G	ENSP00000435866.1:p.Trp804Gly
NM_001243254.1:c.2410T>G	NP_001230183.1:p.Trp804Gly
NM_015213.3:c.2410T>G	NP_056028.2:p.Trp804Gly
XM_005252832.1:c.2410T>G	XP_005252889.1:p.Trp804Gly
XM_011519952.1:c.2410T>G	XP_011518254.1:p.Trp804Gly
XM_011519953.1:c.508T>G	XP_011518255.1:p.Trp170Gly
XR_242782.2:n.2675T>G
XR_930851.1:n.2675T>G
XR_930852.1:n.2675T>G
XR_930853.1:n.2524T>G
NM_001348749.1:c.2338T>G	NP_001335678.1:p.Trp780Gly
NM_001348750.1:c.2122T>G	NP_001335679.1:p.Trp708Gly
NR_145966.2:n.2667T>G
NM_015213.4:c.2410T>G MANE Select	NP_056028.2:p.Trp804Gly
NM_001243254.2:c.2410T>G	NP_001230183.1:p.Trp804Gly
NM_001348749.2:c.2338T>G	NP_001335678.1:p.Trp780Gly
NM_001348750.2:c.2122T>G	NP_001335679.1:p.Trp708Gly