Canonical Allele Identifier: CA379597665

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163565A>G (hg19) ; chr11:g.9142018A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142018A>G , CM000673.2:g.9142018A>G	GRCh38
NC_000011.9:g.9163565A>G , CM000673.1:g.9163565A>G	GRCh37
NC_000011.8:g.9120141A>G	NCBI36
NG_053019.1:g.128318T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3602T>C MANE Select	ENSP00000328524.3:p.Phe1201Ser
ENST00000525784.6:n.1464T>C
ENST00000530780.2:c.*3428T>C	ENSP00000433925.1:n.*3428T>C
ENST00000531747.2:n.3273T>C
ENST00000679446.1:n.3523T>C
ENST00000679458.1:n.5003T>C
ENST00000679460.1:n.4664T>C
ENST00000679568.1:c.3602T>C	ENSP00000505860.1:p.Phe1201Ser
ENST00000679745.1:n.4107T>C
ENST00000679773.1:n.2763T>C
ENST00000679926.1:n.4904T>C
ENST00000679999.1:c.*659T>C	ENSP00000505198.1:n.*659T>C
ENST00000680252.1:c.3269T>C
ENST00000680294.1:c.3395T>C	ENSP00000506113.1:p.Phe1132Ser
ENST00000680358.1:n.2901T>C
ENST00000680470.1:c.*1383T>C	ENSP00000505975.1:n.*1383T>C
ENST00000680554.1:c.*135T>C	ENSP00000505621.1:n.*135T>C
ENST00000680576.1:n.5078T>C
ENST00000680599.1:n.3643T>C
ENST00000680742.1:c.*135T>C	ENSP00000505206.1:n.*135T>C
ENST00000680791.1:n.2486T>C
ENST00000680885.1:n.5304T>C
ENST00000681158.1:c.3186T>C
ENST00000681203.1:c.3530T>C	ENSP00000506456.1:p.Phe1177Ser
ENST00000681371.1:n.3474T>C
ENST00000681425.1:n.4080T>C
ENST00000681639.1:n.1881T>C
ENST00000328194.7:c.3602T>C	ENSP00000328524.3:p.Phe1201Ser
ENST00000525784.5:c.538T>C
ENST00000527700.5:n.3164T>C
ENST00000528725.5:c.298T>C
ENST00000529977.5:n.1503T>C
ENST00000530044.5:c.3602T>C	ENSP00000435866.1:p.Phe1201Ser
ENST00000531747.1:c.838T>C
ENST00000533737.5:c.265T>C
NM_001243254.1:c.3602T>C	NP_001230183.1:p.Phe1201Ser
NM_015213.3:c.3602T>C	NP_056028.2:p.Phe1201Ser
XM_005252832.1:c.3602T>C	XP_005252889.1:p.Phe1201Ser
XM_011519952.1:c.3602T>C	XP_011518254.1:p.Phe1201Ser
XM_011519953.1:c.1700T>C	XP_011518255.1:p.Phe567Ser
XR_242782.2:n.3784T>C
XR_930851.1:n.3784T>C
NM_001348749.1:c.3530T>C	NP_001335678.1:p.Phe1177Ser
NM_001348750.1:c.3314T>C	NP_001335679.1:p.Phe1105Ser
NR_145966.2:n.3776T>C
NM_015213.4:c.3602T>C MANE Select	NP_056028.2:p.Phe1201Ser
NM_001243254.2:c.3602T>C	NP_001230183.1:p.Phe1201Ser
NM_001348749.2:c.3530T>C	NP_001335678.1:p.Phe1177Ser
NM_001348750.2:c.3314T>C	NP_001335679.1:p.Phe1105Ser