Canonical Allele Identifier: CA379597741

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163574A>G (hg19) ; chr11:g.9142027A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142027A>G , CM000673.2:g.9142027A>G	GRCh38
NC_000011.9:g.9163574A>G , CM000673.1:g.9163574A>G	GRCh37
NC_000011.8:g.9120150A>G	NCBI36
NG_053019.1:g.128309T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3593T>C MANE Select	ENSP00000328524.3:p.Phe1198Ser
ENST00000525784.6:n.1455T>C
ENST00000530780.2:c.*3419T>C	ENSP00000433925.1:n.*3419T>C
ENST00000531747.2:n.3264T>C
ENST00000679446.1:n.3514T>C
ENST00000679458.1:n.4994T>C
ENST00000679460.1:n.4655T>C
ENST00000679568.1:c.3593T>C	ENSP00000505860.1:p.Phe1198Ser
ENST00000679745.1:n.4098T>C
ENST00000679773.1:n.2754T>C
ENST00000679926.1:n.4895T>C
ENST00000679999.1:c.*650T>C	ENSP00000505198.1:n.*650T>C
ENST00000680252.1:c.3260T>C
ENST00000680294.1:c.3386T>C	ENSP00000506113.1:p.Phe1129Ser
ENST00000680358.1:n.2892T>C
ENST00000680470.1:c.*1374T>C	ENSP00000505975.1:n.*1374T>C
ENST00000680554.1:c.*126T>C	ENSP00000505621.1:n.*126T>C
ENST00000680576.1:n.5069T>C
ENST00000680599.1:n.3634T>C
ENST00000680742.1:c.*126T>C	ENSP00000505206.1:n.*126T>C
ENST00000680791.1:n.2477T>C
ENST00000680885.1:n.5295T>C
ENST00000681158.1:c.3177T>C
ENST00000681203.1:c.3521T>C	ENSP00000506456.1:p.Phe1174Ser
ENST00000681371.1:n.3465T>C
ENST00000681425.1:n.4071T>C
ENST00000681639.1:n.1872T>C
ENST00000328194.7:c.3593T>C	ENSP00000328524.3:p.Phe1198Ser
ENST00000525784.5:c.529T>C
ENST00000527700.5:n.3155T>C
ENST00000528725.5:c.289T>C
ENST00000529977.5:n.1494T>C
ENST00000530044.5:c.3593T>C	ENSP00000435866.1:p.Phe1198Ser
ENST00000531747.1:c.829T>C
ENST00000533737.5:c.256T>C
NM_001243254.1:c.3593T>C	NP_001230183.1:p.Phe1198Ser
NM_015213.3:c.3593T>C	NP_056028.2:p.Phe1198Ser
XM_005252832.1:c.3593T>C	XP_005252889.1:p.Phe1198Ser
XM_011519952.1:c.3593T>C	XP_011518254.1:p.Phe1198Ser
XM_011519953.1:c.1691T>C	XP_011518255.1:p.Phe564Ser
XR_242782.2:n.3775T>C
XR_930851.1:n.3775T>C
NM_001348749.1:c.3521T>C	NP_001335678.1:p.Phe1174Ser
NM_001348750.1:c.3305T>C	NP_001335679.1:p.Phe1102Ser
NR_145966.2:n.3767T>C
NM_015213.4:c.3593T>C MANE Select	NP_056028.2:p.Phe1198Ser
NM_001243254.2:c.3593T>C	NP_001230183.1:p.Phe1198Ser
NM_001348749.2:c.3521T>C	NP_001335678.1:p.Phe1174Ser
NM_001348750.2:c.3305T>C	NP_001335679.1:p.Phe1102Ser