Canonical Allele Identifier: CA217547613

Gene: DENND5A

Linked Data

• dbSNP Id: rs1036964220
• MyVariant Identifiers: chr11:g.9182400G>A (hg19) ; chr11:g.9160853G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160853G>A , CM000673.2:g.9160853G>A	GRCh38
NC_000011.9:g.9182400G>A , CM000673.1:g.9182400G>A	GRCh37
NC_000011.8:g.9138976G>A	NCBI36
NG_053019.1:g.109483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2296C>T MANE Select	ENSP00000328524.3:p.Leu766=
ENST00000530780.2:c.*2122C>T	ENSP00000433925.1:n.*2122C>T
ENST00000679446.1:n.2217C>T
ENST00000679458.1:n.3697C>T
ENST00000679460.1:n.2085C>T
ENST00000679568.1:c.2296C>T	ENSP00000505860.1:p.Leu766=
ENST00000679745.1:n.2085C>T
ENST00000679926.1:n.1112C>T
ENST00000679999.1:c.2296C>T	ENSP00000505198.1:p.Leu766=
ENST00000680252.1:c.2085C>T
ENST00000680294.1:c.2296C>T	ENSP00000506113.1:p.Leu766=
ENST00000680358.1:n.1595C>T
ENST00000680470.1:c.*162C>T	ENSP00000505975.1:n.*162C>T
ENST00000680554.1:c.2008C>T	ENSP00000505621.1:p.Leu670=
ENST00000680576.1:n.2085C>T
ENST00000680599.1:n.2213C>T
ENST00000680742.1:c.2296C>T	ENSP00000505206.1:p.Leu766=
ENST00000680885.1:n.2217C>T
ENST00000681158.1:c.2085C>T
ENST00000681173.1:n.2085C>T
ENST00000681203.1:c.2224C>T	ENSP00000506456.1:p.Leu742=
ENST00000681425.1:n.2217C>T
ENST00000328194.7:c.2296C>T	ENSP00000328524.3:p.Leu766=
ENST00000526707.5:c.2224C>T	ENSP00000436780.1:p.Leu742=
ENST00000527700.5:n.1858C>T
ENST00000530044.5:c.2296C>T	ENSP00000435866.1:p.Leu766=
NM_001243254.1:c.2296C>T	NP_001230183.1:p.Leu766=
NM_015213.3:c.2296C>T	NP_056028.2:p.Leu766=
XM_005252832.1:c.2296C>T	XP_005252889.1:p.Leu766=
XM_011519952.1:c.2296C>T	XP_011518254.1:p.Leu766=
XM_011519953.1:c.394C>T	XP_011518255.1:p.Leu132=
XR_242782.2:n.2561C>T
XR_930851.1:n.2561C>T
XR_930852.1:n.2561C>T
XR_930853.1:n.2410C>T
NM_001348749.1:c.2224C>T	NP_001335678.1:p.Leu742=
NM_001348750.1:c.2008C>T	NP_001335679.1:p.Leu670=
NR_145966.2:n.2553C>T
NM_015213.4:c.2296C>T MANE Select	NP_056028.2:p.Leu766=
NM_001243254.2:c.2296C>T	NP_001230183.1:p.Leu766=
NM_001348749.2:c.2224C>T	NP_001335678.1:p.Leu742=
NM_001348750.2:c.2008C>T	NP_001335679.1:p.Leu670=