Canonical Allele Identifier: CA473040270

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9142095-G-A
• MyVariant Identifiers: chr11:g.9163642G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142095G>A , CM000673.2:g.9142095G>A	GRCh38
NC_000011.9:g.9163642G>A , CM000673.1:g.9163642G>A	GRCh37
NC_000011.8:g.9120218G>A	NCBI36
NG_053019.1:g.128241C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3525C>T MANE Select	ENSP00000328524.3:p.Thr1175=
ENST00000525784.6:n.1387C>T
ENST00000530780.2:c.*3351C>T	ENSP00000433925.1:n.*3351C>T
ENST00000531747.2:n.3196C>T
ENST00000679446.1:n.3446C>T
ENST00000679458.1:n.4926C>T
ENST00000679460.1:n.4587C>T
ENST00000679568.1:c.3525C>T	ENSP00000505860.1:p.Thr1175=
ENST00000679745.1:n.4030C>T
ENST00000679773.1:n.2686C>T
ENST00000679926.1:n.4827C>T
ENST00000679999.1:c.*582C>T	ENSP00000505198.1:n.*582C>T
ENST00000680252.1:c.3192C>T
ENST00000680294.1:c.3318C>T	ENSP00000506113.1:p.Thr1106=
ENST00000680358.1:n.2824C>T
ENST00000680470.1:c.*1306C>T	ENSP00000505975.1:n.*1306C>T
ENST00000680554.1:c.*58C>T	ENSP00000505621.1:n.*58C>T
ENST00000680576.1:n.5001C>T
ENST00000680599.1:n.3566C>T
ENST00000680742.1:c.*58C>T	ENSP00000505206.1:n.*58C>T
ENST00000680791.1:n.2409C>T
ENST00000680885.1:n.5227C>T
ENST00000681158.1:c.3109C>T
ENST00000681203.1:c.3453C>T	ENSP00000506456.1:p.Thr1151=
ENST00000681371.1:n.3397C>T
ENST00000681425.1:n.4003C>T
ENST00000681639.1:n.1804C>T
ENST00000328194.7:c.3525C>T	ENSP00000328524.3:p.Thr1175=
ENST00000525784.5:c.461C>T
ENST00000527700.5:n.3087C>T
ENST00000528725.5:c.221C>T
ENST00000529977.5:n.1426C>T
ENST00000530044.5:c.3525C>T	ENSP00000435866.1:p.Thr1175=
ENST00000531747.1:c.761C>T
ENST00000533737.5:c.188C>T
NM_001243254.1:c.3525C>T	NP_001230183.1:p.Thr1175=
NM_015213.3:c.3525C>T	NP_056028.2:p.Thr1175=
XM_005252832.1:c.3525C>T	XP_005252889.1:p.Thr1175=
XM_011519952.1:c.3525C>T	XP_011518254.1:p.Thr1175=
XM_011519953.1:c.1623C>T	XP_011518255.1:p.Thr541=
XR_242782.2:n.3707C>T
XR_930851.1:n.3707C>T
NM_001348749.1:c.3453C>T	NP_001335678.1:p.Thr1151=
NM_001348750.1:c.3237C>T	NP_001335679.1:p.Thr1079=
NR_145966.2:n.3699C>T
NM_015213.4:c.3525C>T MANE Select	NP_056028.2:p.Thr1175=
NM_001243254.2:c.3525C>T	NP_001230183.1:p.Thr1175=
NM_001348749.2:c.3453C>T	NP_001335678.1:p.Thr1151=
NM_001348750.2:c.3237C>T	NP_001335679.1:p.Thr1079=