Canonical Allele Identifier: CA379598199

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163640T>A (hg19) ; chr11:g.9142093T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142093T>A , CM000673.2:g.9142093T>A	GRCh38
NC_000011.9:g.9163640T>A , CM000673.1:g.9163640T>A	GRCh37
NC_000011.8:g.9120216T>A	NCBI36
NG_053019.1:g.128243A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3527A>T MANE Select	ENSP00000328524.3:p.Tyr1176Phe
ENST00000525784.6:n.1389A>T
ENST00000530780.2:c.*3353A>T	ENSP00000433925.1:n.*3353A>T
ENST00000531747.2:n.3198A>T
ENST00000679446.1:n.3448A>T
ENST00000679458.1:n.4928A>T
ENST00000679460.1:n.4589A>T
ENST00000679568.1:c.3527A>T	ENSP00000505860.1:p.Tyr1176Phe
ENST00000679745.1:n.4032A>T
ENST00000679773.1:n.2688A>T
ENST00000679926.1:n.4829A>T
ENST00000679999.1:c.*584A>T	ENSP00000505198.1:n.*584A>T
ENST00000680252.1:c.3194A>T
ENST00000680294.1:c.3320A>T	ENSP00000506113.1:p.Tyr1107Phe
ENST00000680358.1:n.2826A>T
ENST00000680470.1:c.*1308A>T	ENSP00000505975.1:n.*1308A>T
ENST00000680554.1:c.*60A>T	ENSP00000505621.1:n.*60A>T
ENST00000680576.1:n.5003A>T
ENST00000680599.1:n.3568A>T
ENST00000680742.1:c.*60A>T	ENSP00000505206.1:n.*60A>T
ENST00000680791.1:n.2411A>T
ENST00000680885.1:n.5229A>T
ENST00000681158.1:c.3111A>T
ENST00000681203.1:c.3455A>T	ENSP00000506456.1:p.Tyr1152Phe
ENST00000681371.1:n.3399A>T
ENST00000681425.1:n.4005A>T
ENST00000681639.1:n.1806A>T
ENST00000328194.7:c.3527A>T	ENSP00000328524.3:p.Tyr1176Phe
ENST00000525784.5:c.463A>T
ENST00000527700.5:n.3089A>T
ENST00000528725.5:c.223A>T
ENST00000529977.5:n.1428A>T
ENST00000530044.5:c.3527A>T	ENSP00000435866.1:p.Tyr1176Phe
ENST00000531747.1:c.763A>T
ENST00000533737.5:c.190A>T
NM_001243254.1:c.3527A>T	NP_001230183.1:p.Tyr1176Phe
NM_015213.3:c.3527A>T	NP_056028.2:p.Tyr1176Phe
XM_005252832.1:c.3527A>T	XP_005252889.1:p.Tyr1176Phe
XM_011519952.1:c.3527A>T	XP_011518254.1:p.Tyr1176Phe
XM_011519953.1:c.1625A>T	XP_011518255.1:p.Tyr542Phe
XR_242782.2:n.3709A>T
XR_930851.1:n.3709A>T
NM_001348749.1:c.3455A>T	NP_001335678.1:p.Tyr1152Phe
NM_001348750.1:c.3239A>T	NP_001335679.1:p.Tyr1080Phe
NR_145966.2:n.3701A>T
NM_015213.4:c.3527A>T MANE Select	NP_056028.2:p.Tyr1176Phe
NM_001243254.2:c.3527A>T	NP_001230183.1:p.Tyr1176Phe
NM_001348749.2:c.3455A>T	NP_001335678.1:p.Tyr1152Phe
NM_001348750.2:c.3239A>T	NP_001335679.1:p.Tyr1080Phe