Canonical Allele Identifier: CA4896737

Gene: DENND3

Linked Data

• dbSNP Id: rs752897055
• ExAC: 8:142178089 CCT / C
• gnomAD v2: 8-142178089-CCT-C
• gnomAD v3: 8-141167990-CCT-C
• gnomAD v4: 8-141167990-CCT-C
• MyVariant Identifiers: chr8:g.142178090_142178091del (hg19) ; chr8:g.141167991_141167992del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141167991_141167992del , CM000670.2:g.141167991_141167992del	GRCh38
NC_000008.10:g.142178090_142178091del , CM000670.1:g.142178090_142178091del	GRCh37
NC_000008.9:g.142247272_142247273del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1754-13_1754-12del MANE Select	ENSP00000428714.1:n.1754-13_1754-12del
ENST00000262585.6:c.1514-13_1514-12del	ENSP00000262585.2:n.1514-13_1514-12del
ENST00000424248.2:c.1358-13_1358-12del	ENSP00000410594.1:n.1358-13_1358-12del
ENST00000518668.5:c.1527-13_1527-12del
ENST00000519811.5:c.1754-13_1754-12del	ENSP00000428714.1:n.1754-13_1754-12del
ENST00000520482.1:n.1295-13_1295-12del
NM_014957.2:c.1514-13_1514-12del	NP_055772.2:n.1514-13_1514-12del
XM_005250838.3:c.1553-13_1553-12del	XP_005250895.2:n.1553-13_1553-12del
XM_005250839.2:c.1553-13_1553-12del	XP_005250896.2:n.1553-13_1553-12del
XM_005250840.3:c.1397-13_1397-12del	XP_005250897.2:n.1397-13_1397-12del
XM_005250841.2:c.1397-13_1397-12del	XP_005250898.2:n.1397-13_1397-12del
XM_005250842.3:c.1520-13_1520-12del	XP_005250899.1:n.1520-13_1520-12del
XM_005250843.3:c.1010-13_1010-12del	XP_005250900.1:n.1010-13_1010-12del
XM_011516933.1:c.1553-13_1553-12del	XP_011515235.1:n.1553-13_1553-12del
XM_011516934.1:c.1553-13_1553-12del	XP_011515236.1:n.1553-13_1553-12del
XM_011516935.1:c.1187-13_1187-12del	XP_011515237.1:n.1187-13_1187-12del
XM_011516936.1:c.1181-13_1181-12del	XP_011515238.1:n.1181-13_1181-12del
XM_011516937.1:c.1553-13_1553-12del	XP_011515239.1:n.1553-13_1553-12del
XM_011516938.1:c.722-13_722-12del	XP_011515240.1:n.722-13_722-12del
XM_011516939.1:c.251-13_251-12del	XP_011515241.1:n.251-13_251-12del
XM_011516940.1:c.251-13_251-12del	XP_011515242.1:n.251-13_251-12del
XM_011516941.1:c.1553-13_1553-12del	XP_011515243.1:n.1553-13_1553-12del
XM_011516942.1:c.1553-13_1553-12del	XP_011515244.1:n.1553-13_1553-12del
XR_242384.2:n.1683-13_1683-12del
XR_928310.1:n.1683-13_1683-12del
XR_928311.1:n.1683-13_1683-12del
XR_928312.1:n.1683-13_1683-12del
NM_001352890.2:c.1754-13_1754-12del	NP_001339819.2:n.1754-13_1754-12del
NM_001362798.1:c.1754-13_1754-12del	NP_001349727.1:n.1754-13_1754-12del
NM_014957.4:c.1553-13_1553-12del	NP_055772.3:n.1553-13_1553-12del
NR_148197.2:n.1850-13_1850-12del
XM_005250840.5:c.1598-13_1598-12del	XP_005250897.3:n.1598-13_1598-12del
XM_005250841.4:c.1598-13_1598-12del	XP_005250898.3:n.1598-13_1598-12del
XM_005250842.4:c.1520-13_1520-12del	XP_005250899.1:n.1520-13_1520-12del
XM_011516933.2:c.1754-13_1754-12del	XP_011515235.2:n.1754-13_1754-12del
XM_011516934.3:c.1754-13_1754-12del	XP_011515236.2:n.1754-13_1754-12del
XM_011516937.2:c.1754-13_1754-12del	XP_011515239.2:n.1754-13_1754-12del
XM_011516938.3:c.722-13_722-12del	XP_011515240.1:n.722-13_722-12del
XM_011516939.3:c.251-13_251-12del	XP_011515241.1:n.251-13_251-12del
XM_011516940.2:c.251-13_251-12del	XP_011515242.1:n.251-13_251-12del
XM_011516941.3:c.1754-13_1754-12del	XP_011515243.2:n.1754-13_1754-12del
XM_017013241.1:c.1553-13_1553-12del	XP_016868730.1:n.1553-13_1553-12del
XM_017013242.1:c.1010-13_1010-12del	XP_016868731.1:n.1010-13_1010-12del
XM_017013243.1:c.290-13_290-12del	XP_016868732.1:n.290-13_290-12del
XR_001745497.2:n.1900-13_1900-12del
XR_001745498.2:n.1900-13_1900-12del
XR_928310.3:n.1900-13_1900-12del
XR_928312.3:n.1900-13_1900-12del
NM_001352890.3:c.1754-13_1754-12del MANE Select	NP_001339819.2:n.1754-13_1754-12del
NM_001362798.2:c.1754-13_1754-12del	NP_001349727.1:n.1754-13_1754-12del
NM_014957.5:c.1553-13_1553-12del	NP_055772.3:n.1553-13_1553-12del
NR_148197.3:n.1873-13_1873-12del