Canonical Allele Identifier: CA1951454158

Gene: DENND5A

Linked Data

• dbSNP Id: rs1847268486
• gnomAD v4: 11-9142173-GCCAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142174_9142177del , CM000673.2:g.9142174_9142177del	GRCh38
NC_000011.9:g.9163721_9163724del , CM000673.1:g.9163721_9163724del	GRCh37
NC_000011.8:g.9120297_9120300del	NCBI36
NG_053019.1:g.128159_128162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3512-69_3512-66del MANE Select	ENSP00000328524.3:n.3512-69_3512-66del
ENST00000525784.6:n.1374-69_1374-66del
ENST00000530780.2:c.*3338-69_*3338-66del	ENSP00000433925.1:n.*3338-69_*3338-66del
ENST00000531747.2:n.3183-69_3183-66del
ENST00000679446.1:n.3433-69_3433-66del
ENST00000679458.1:n.4913-69_4913-66del
ENST00000679460.1:n.4574-69_4574-66del
ENST00000679568.1:c.3512-69_3512-66del	ENSP00000505860.1:n.3512-69_3512-66del
ENST00000679745.1:n.4017-69_4017-66del
ENST00000679773.1:n.2673-69_2673-66del
ENST00000679926.1:n.4814-69_4814-66del
ENST00000679999.1:c.*569-69_*569-66del	ENSP00000505198.1:n.*569-69_*569-66del
ENST00000680252.1:c.3179-69_3179-66del
ENST00000680294.1:c.3305-69_3305-66del	ENSP00000506113.1:n.3305-69_3305-66del
ENST00000680358.1:n.2811-69_2811-66del
ENST00000680470.1:c.*1293-69_*1293-66del	ENSP00000505975.1:n.*1293-69_*1293-66del
ENST00000680554.1:c.*45-69_*45-66del	ENSP00000505621.1:n.*45-69_*45-66del
ENST00000680576.1:n.4988-69_4988-66del
ENST00000680599.1:n.3553-69_3553-66del
ENST00000680742.1:c.*45-69_*45-66del	ENSP00000505206.1:n.*45-69_*45-66del
ENST00000680791.1:n.2396-69_2396-66del
ENST00000680885.1:n.5145_5148del
ENST00000681158.1:c.3096-69_3096-66del
ENST00000681203.1:c.3440-69_3440-66del	ENSP00000506456.1:n.3440-69_3440-66del
ENST00000681371.1:n.3384-69_3384-66del
ENST00000681425.1:n.3990-69_3990-66del
ENST00000681639.1:n.1722_1725del
ENST00000328194.7:c.3512-69_3512-66del	ENSP00000328524.3:n.3512-69_3512-66del
ENST00000525784.5:c.448-69_448-66del
ENST00000527700.5:n.3074-69_3074-66del
ENST00000528725.5:c.208-69_208-66del
ENST00000529977.5:n.1413-69_1413-66del
ENST00000530044.5:c.3512-69_3512-66del	ENSP00000435866.1:n.3512-69_3512-66del
ENST00000531747.1:c.748-69_748-66del
ENST00000533737.5:c.175-69_175-66del
NM_001243254.1:c.3512-69_3512-66del	NP_001230183.1:n.3512-69_3512-66del
NM_015213.3:c.3512-69_3512-66del	NP_056028.2:n.3512-69_3512-66del
XM_005252832.1:c.3512-69_3512-66del	XP_005252889.1:n.3512-69_3512-66del
XM_011519952.1:c.3512-69_3512-66del	XP_011518254.1:n.3512-69_3512-66del
XM_011519953.1:c.1610-69_1610-66del	XP_011518255.1:n.1610-69_1610-66del
XR_242782.2:n.3694-69_3694-66del
XR_930851.1:n.3694-69_3694-66del
NM_001348749.1:c.3440-69_3440-66del	NP_001335678.1:n.3440-69_3440-66del
NM_001348750.1:c.3224-69_3224-66del	NP_001335679.1:n.3224-69_3224-66del
NR_145966.2:n.3686-69_3686-66del
NM_015213.4:c.3512-69_3512-66del MANE Select	NP_056028.2:n.3512-69_3512-66del
NM_001243254.2:c.3512-69_3512-66del	NP_001230183.1:n.3512-69_3512-66del
NM_001348749.2:c.3440-69_3440-66del	NP_001335678.1:n.3440-69_3440-66del
NM_001348750.2:c.3224-69_3224-66del	NP_001335679.1:n.3224-69_3224-66del