Canonical Allele Identifier: CA473044083

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182296C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160749C>A , CM000673.2:g.9160749C>A	GRCh38
NC_000011.9:g.9182296C>A , CM000673.1:g.9182296C>A	GRCh37
NC_000011.8:g.9138872C>A	NCBI36
NG_053019.1:g.109587G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2400G>T MANE Select	ENSP00000328524.3:p.Leu800=
ENST00000530780.2:c.*2226G>T	ENSP00000433925.1:n.*2226G>T
ENST00000679446.1:n.2321G>T
ENST00000679458.1:n.3801G>T
ENST00000679460.1:n.2189G>T
ENST00000679568.1:c.2400G>T	ENSP00000505860.1:p.Leu800=
ENST00000679745.1:n.2189G>T
ENST00000679926.1:n.1216G>T
ENST00000679999.1:c.2400G>T	ENSP00000505198.1:p.Leu800=
ENST00000680252.1:c.2189G>T
ENST00000680294.1:c.2400G>T	ENSP00000506113.1:p.Leu800=
ENST00000680358.1:n.1699G>T
ENST00000680470.1:c.*266G>T	ENSP00000505975.1:n.*266G>T
ENST00000680554.1:c.2112G>T	ENSP00000505621.1:p.Leu704=
ENST00000680576.1:n.2189G>T
ENST00000680599.1:n.2317G>T
ENST00000680742.1:c.2400G>T	ENSP00000505206.1:p.Leu800=
ENST00000680885.1:n.2321G>T
ENST00000681158.1:c.2189G>T
ENST00000681173.1:n.2189G>T
ENST00000681203.1:c.2328G>T	ENSP00000506456.1:p.Leu776=
ENST00000681425.1:n.2321G>T
ENST00000328194.7:c.2400G>T	ENSP00000328524.3:p.Leu800=
ENST00000526707.5:c.2328G>T	ENSP00000436780.1:p.Leu776=
ENST00000527700.5:n.1962G>T
ENST00000530044.5:c.2400G>T	ENSP00000435866.1:p.Leu800=
NM_001243254.1:c.2400G>T	NP_001230183.1:p.Leu800=
NM_015213.3:c.2400G>T	NP_056028.2:p.Leu800=
XM_005252832.1:c.2400G>T	XP_005252889.1:p.Leu800=
XM_011519952.1:c.2400G>T	XP_011518254.1:p.Leu800=
XM_011519953.1:c.498G>T	XP_011518255.1:p.Leu166=
XR_242782.2:n.2665G>T
XR_930851.1:n.2665G>T
XR_930852.1:n.2665G>T
XR_930853.1:n.2514G>T
NM_001348749.1:c.2328G>T	NP_001335678.1:p.Leu776=
NM_001348750.1:c.2112G>T	NP_001335679.1:p.Leu704=
NR_145966.2:n.2657G>T
NM_015213.4:c.2400G>T MANE Select	NP_056028.2:p.Leu800=
NM_001243254.2:c.2400G>T	NP_001230183.1:p.Leu800=
NM_001348749.2:c.2328G>T	NP_001335678.1:p.Leu776=
NM_001348750.2:c.2112G>T	NP_001335679.1:p.Leu704=