Canonical Allele Identifier: CA379598031

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163610A>G (hg19) ; chr11:g.9142063A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142063A>G , CM000673.2:g.9142063A>G	GRCh38
NC_000011.9:g.9163610A>G , CM000673.1:g.9163610A>G	GRCh37
NC_000011.8:g.9120186A>G	NCBI36
NG_053019.1:g.128273T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3557T>C MANE Select	ENSP00000328524.3:p.Val1186Ala
ENST00000525784.6:n.1419T>C
ENST00000530780.2:c.*3383T>C	ENSP00000433925.1:n.*3383T>C
ENST00000531747.2:n.3228T>C
ENST00000679446.1:n.3478T>C
ENST00000679458.1:n.4958T>C
ENST00000679460.1:n.4619T>C
ENST00000679568.1:c.3557T>C	ENSP00000505860.1:p.Val1186Ala
ENST00000679745.1:n.4062T>C
ENST00000679773.1:n.2718T>C
ENST00000679926.1:n.4859T>C
ENST00000679999.1:c.*614T>C	ENSP00000505198.1:n.*614T>C
ENST00000680252.1:c.3224T>C
ENST00000680294.1:c.3350T>C	ENSP00000506113.1:p.Val1117Ala
ENST00000680358.1:n.2856T>C
ENST00000680470.1:c.*1338T>C	ENSP00000505975.1:n.*1338T>C
ENST00000680554.1:c.*90T>C	ENSP00000505621.1:n.*90T>C
ENST00000680576.1:n.5033T>C
ENST00000680599.1:n.3598T>C
ENST00000680742.1:c.*90T>C	ENSP00000505206.1:n.*90T>C
ENST00000680791.1:n.2441T>C
ENST00000680885.1:n.5259T>C
ENST00000681158.1:c.3141T>C
ENST00000681203.1:c.3485T>C	ENSP00000506456.1:p.Val1162Ala
ENST00000681371.1:n.3429T>C
ENST00000681425.1:n.4035T>C
ENST00000681639.1:n.1836T>C
ENST00000328194.7:c.3557T>C	ENSP00000328524.3:p.Val1186Ala
ENST00000525784.5:c.493T>C
ENST00000527700.5:n.3119T>C
ENST00000528725.5:c.253T>C
ENST00000529977.5:n.1458T>C
ENST00000530044.5:c.3557T>C	ENSP00000435866.1:p.Val1186Ala
ENST00000531747.1:c.793T>C
ENST00000533737.5:c.220T>C
NM_001243254.1:c.3557T>C	NP_001230183.1:p.Val1186Ala
NM_015213.3:c.3557T>C	NP_056028.2:p.Val1186Ala
XM_005252832.1:c.3557T>C	XP_005252889.1:p.Val1186Ala
XM_011519952.1:c.3557T>C	XP_011518254.1:p.Val1186Ala
XM_011519953.1:c.1655T>C	XP_011518255.1:p.Val552Ala
XR_242782.2:n.3739T>C
XR_930851.1:n.3739T>C
NM_001348749.1:c.3485T>C	NP_001335678.1:p.Val1162Ala
NM_001348750.1:c.3269T>C	NP_001335679.1:p.Val1090Ala
NR_145966.2:n.3731T>C
NM_015213.4:c.3557T>C MANE Select	NP_056028.2:p.Val1186Ala
NM_001243254.2:c.3557T>C	NP_001230183.1:p.Val1186Ala
NM_001348749.2:c.3485T>C	NP_001335678.1:p.Val1162Ala
NM_001348750.2:c.3269T>C	NP_001335679.1:p.Val1090Ala