Canonical Allele Identifier: CA379597767

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163578T>A (hg19) ; chr11:g.9142031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142031T>A , CM000673.2:g.9142031T>A	GRCh38
NC_000011.9:g.9163578T>A , CM000673.1:g.9163578T>A	GRCh37
NC_000011.8:g.9120154T>A	NCBI36
NG_053019.1:g.128305A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3589A>T MANE Select	ENSP00000328524.3:p.Asn1197Tyr
ENST00000525784.6:n.1451A>T
ENST00000530780.2:c.*3415A>T	ENSP00000433925.1:n.*3415A>T
ENST00000531747.2:n.3260A>T
ENST00000679446.1:n.3510A>T
ENST00000679458.1:n.4990A>T
ENST00000679460.1:n.4651A>T
ENST00000679568.1:c.3589A>T	ENSP00000505860.1:p.Asn1197Tyr
ENST00000679745.1:n.4094A>T
ENST00000679773.1:n.2750A>T
ENST00000679926.1:n.4891A>T
ENST00000679999.1:c.*646A>T	ENSP00000505198.1:n.*646A>T
ENST00000680252.1:c.3256A>T
ENST00000680294.1:c.3382A>T	ENSP00000506113.1:p.Asn1128Tyr
ENST00000680358.1:n.2888A>T
ENST00000680470.1:c.*1370A>T	ENSP00000505975.1:n.*1370A>T
ENST00000680554.1:c.*122A>T	ENSP00000505621.1:n.*122A>T
ENST00000680576.1:n.5065A>T
ENST00000680599.1:n.3630A>T
ENST00000680742.1:c.*122A>T	ENSP00000505206.1:n.*122A>T
ENST00000680791.1:n.2473A>T
ENST00000680885.1:n.5291A>T
ENST00000681158.1:c.3173A>T
ENST00000681203.1:c.3517A>T	ENSP00000506456.1:p.Asn1173Tyr
ENST00000681371.1:n.3461A>T
ENST00000681425.1:n.4067A>T
ENST00000681639.1:n.1868A>T
ENST00000328194.7:c.3589A>T	ENSP00000328524.3:p.Asn1197Tyr
ENST00000525784.5:c.525A>T
ENST00000527700.5:n.3151A>T
ENST00000528725.5:c.285A>T
ENST00000529977.5:n.1490A>T
ENST00000530044.5:c.3589A>T	ENSP00000435866.1:p.Asn1197Tyr
ENST00000531747.1:c.825A>T
ENST00000533737.5:c.252A>T
NM_001243254.1:c.3589A>T	NP_001230183.1:p.Asn1197Tyr
NM_015213.3:c.3589A>T	NP_056028.2:p.Asn1197Tyr
XM_005252832.1:c.3589A>T	XP_005252889.1:p.Asn1197Tyr
XM_011519952.1:c.3589A>T	XP_011518254.1:p.Asn1197Tyr
XM_011519953.1:c.1687A>T	XP_011518255.1:p.Asn563Tyr
XR_242782.2:n.3771A>T
XR_930851.1:n.3771A>T
NM_001348749.1:c.3517A>T	NP_001335678.1:p.Asn1173Tyr
NM_001348750.1:c.3301A>T	NP_001335679.1:p.Asn1101Tyr
NR_145966.2:n.3763A>T
NM_015213.4:c.3589A>T MANE Select	NP_056028.2:p.Asn1197Tyr
NM_001243254.2:c.3589A>T	NP_001230183.1:p.Asn1197Tyr
NM_001348749.2:c.3517A>T	NP_001335678.1:p.Asn1173Tyr
NM_001348750.2:c.3301A>T	NP_001335679.1:p.Asn1101Tyr