Canonical Allele Identifier: CA217547894

Gene: DENND5A

Linked Data

• ClinVar Variation Id: 1927693
• ClinVar RCV Id: RCV002621823
• dbSNP Id: rs893222199
• gnomAD v2: 11-9225742-A-G
• gnomAD v3: 11-9204195-A-G
• gnomAD v4: 11-9204195-A-G
• MyVariant Identifiers: chr11:g.9225742A>G (hg19) ; chr11:g.9204195A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204195A>G , CM000673.2:g.9204195A>G	GRCh38
NC_000011.9:g.9225742A>G , CM000673.1:g.9225742A>G	GRCh37
NC_000011.8:g.9182318A>G	NCBI36
NG_053019.1:g.66141T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.414T>C MANE Select	ENSP00000328524.3:p.Tyr138=
ENST00000530780.2:c.*240T>C	ENSP00000433925.1:n.*240T>C
ENST00000530867.2:n.203T>C
ENST00000532696.2:n.337T>C
ENST00000679446.1:n.335T>C
ENST00000679460.1:n.203T>C
ENST00000679568.1:c.414T>C	ENSP00000505860.1:p.Tyr138=
ENST00000679745.1:n.203T>C
ENST00000679999.1:c.414T>C	ENSP00000505198.1:p.Tyr138=
ENST00000680252.1:c.203T>C
ENST00000680294.1:c.414T>C	ENSP00000506113.1:p.Tyr138=
ENST00000680470.1:c.414T>C	ENSP00000505975.1:p.Tyr138=
ENST00000680554.1:c.126T>C	ENSP00000505621.1:p.Tyr42=
ENST00000680576.1:n.203T>C
ENST00000680599.1:n.331T>C
ENST00000680742.1:c.414T>C	ENSP00000505206.1:p.Tyr138=
ENST00000680885.1:n.335T>C
ENST00000681158.1:c.203T>C
ENST00000681173.1:n.203T>C
ENST00000681203.1:c.342T>C	ENSP00000506456.1:p.Tyr114=
ENST00000681425.1:n.335T>C
ENST00000681915.1:n.203T>C
ENST00000328194.7:c.414T>C	ENSP00000328524.3:p.Tyr138=
ENST00000526707.5:c.342T>C	ENSP00000436780.1:p.Tyr114=
ENST00000530044.5:c.414T>C	ENSP00000435866.1:p.Tyr138=
ENST00000530780.1:c.*240T>C	ENSP00000433925.1:n.*240T>C
ENST00000532696.1:n.169T>C
NM_001243254.1:c.414T>C	NP_001230183.1:p.Tyr138=
NM_015213.3:c.414T>C	NP_056028.2:p.Tyr138=
XM_005252832.1:c.414T>C	XP_005252889.1:p.Tyr138=
XM_011519952.1:c.414T>C	XP_011518254.1:p.Tyr138=
XR_242782.2:n.679T>C
XR_930851.1:n.679T>C
XR_930852.1:n.679T>C
XR_930853.1:n.679T>C
NM_001348749.1:c.342T>C	NP_001335678.1:p.Tyr114=
NM_001348750.1:c.126T>C	NP_001335679.1:p.Tyr42=
NR_145966.2:n.671T>C
NM_015213.4:c.414T>C MANE Select	NP_056028.2:p.Tyr138=
NM_001243254.2:c.414T>C	NP_001230183.1:p.Tyr138=
NM_001348749.2:c.342T>C	NP_001335678.1:p.Tyr114=
NM_001348750.2:c.126T>C	NP_001335679.1:p.Tyr42=