Canonical Allele Identifier: CA473040246

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163588T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142041T>A , CM000673.2:g.9142041T>A	GRCh38
NC_000011.9:g.9163588T>A , CM000673.1:g.9163588T>A	GRCh37
NC_000011.8:g.9120164T>A	NCBI36
NG_053019.1:g.128295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3579A>T MANE Select	ENSP00000328524.3:p.Thr1193=
ENST00000525784.6:n.1441A>T
ENST00000530780.2:c.*3405A>T	ENSP00000433925.1:n.*3405A>T
ENST00000531747.2:n.3250A>T
ENST00000679446.1:n.3500A>T
ENST00000679458.1:n.4980A>T
ENST00000679460.1:n.4641A>T
ENST00000679568.1:c.3579A>T	ENSP00000505860.1:p.Thr1193=
ENST00000679745.1:n.4084A>T
ENST00000679773.1:n.2740A>T
ENST00000679926.1:n.4881A>T
ENST00000679999.1:c.*636A>T	ENSP00000505198.1:n.*636A>T
ENST00000680252.1:c.3246A>T
ENST00000680294.1:c.3372A>T	ENSP00000506113.1:p.Thr1124=
ENST00000680358.1:n.2878A>T
ENST00000680470.1:c.*1360A>T	ENSP00000505975.1:n.*1360A>T
ENST00000680554.1:c.*112A>T	ENSP00000505621.1:n.*112A>T
ENST00000680576.1:n.5055A>T
ENST00000680599.1:n.3620A>T
ENST00000680742.1:c.*112A>T	ENSP00000505206.1:n.*112A>T
ENST00000680791.1:n.2463A>T
ENST00000680885.1:n.5281A>T
ENST00000681158.1:c.3163A>T
ENST00000681203.1:c.3507A>T	ENSP00000506456.1:p.Thr1169=
ENST00000681371.1:n.3451A>T
ENST00000681425.1:n.4057A>T
ENST00000681639.1:n.1858A>T
ENST00000328194.7:c.3579A>T	ENSP00000328524.3:p.Thr1193=
ENST00000525784.5:c.515A>T
ENST00000527700.5:n.3141A>T
ENST00000528725.5:c.275A>T
ENST00000529977.5:n.1480A>T
ENST00000530044.5:c.3579A>T	ENSP00000435866.1:p.Thr1193=
ENST00000531747.1:c.815A>T
ENST00000533737.5:c.242A>T
NM_001243254.1:c.3579A>T	NP_001230183.1:p.Thr1193=
NM_015213.3:c.3579A>T	NP_056028.2:p.Thr1193=
XM_005252832.1:c.3579A>T	XP_005252889.1:p.Thr1193=
XM_011519952.1:c.3579A>T	XP_011518254.1:p.Thr1193=
XM_011519953.1:c.1677A>T	XP_011518255.1:p.Thr559=
XR_242782.2:n.3761A>T
XR_930851.1:n.3761A>T
NM_001348749.1:c.3507A>T	NP_001335678.1:p.Thr1169=
NM_001348750.1:c.3291A>T	NP_001335679.1:p.Thr1097=
NR_145966.2:n.3753A>T
NM_015213.4:c.3579A>T MANE Select	NP_056028.2:p.Thr1193=
NM_001243254.2:c.3579A>T	NP_001230183.1:p.Thr1193=
NM_001348749.2:c.3507A>T	NP_001335678.1:p.Thr1169=
NM_001348750.2:c.3291A>T	NP_001335679.1:p.Thr1097=