Canonical Allele Identifier: CA372344529

Gene: DENND3

Linked Data

• dbSNP Id: rs1458863149
• gnomAD v2: 8-142178574-T-C
• gnomAD v4: 8-141168475-T-C
• MyVariant Identifiers: chr8:g.142178574T>C (hg19) ; chr8:g.141168475T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168475T>C , CM000670.2:g.141168475T>C	GRCh38
NC_000008.10:g.142178574T>C , CM000670.1:g.142178574T>C	GRCh37
NC_000008.9:g.142247756T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2225T>C MANE Select	ENSP00000428714.1:p.Ile742Thr
ENST00000262585.6:c.1985T>C	ENSP00000262585.2:p.Ile662Thr
ENST00000424248.2:c.1829T>C	ENSP00000410594.1:p.Ile610Thr
ENST00000518668.5:c.1998T>C
ENST00000519811.5:c.2225T>C	ENSP00000428714.1:p.Ile742Thr
ENST00000520482.1:n.1766T>C
NM_014957.2:c.1985T>C	NP_055772.2:p.Ile662Thr
XM_005250838.3:c.2024T>C	XP_005250895.2:p.Ile675Thr
XM_005250839.2:c.2024T>C	XP_005250896.2:p.Ile675Thr
XM_005250840.3:c.1868T>C	XP_005250897.2:p.Ile623Thr
XM_005250841.2:c.1868T>C	XP_005250898.2:p.Ile623Thr
XM_005250842.3:c.1991T>C	XP_005250899.1:p.Ile664Thr
XM_005250843.3:c.1481T>C	XP_005250900.1:p.Ile494Thr
XM_011516933.1:c.2024T>C	XP_011515235.1:p.Ile675Thr
XM_011516934.1:c.2024T>C	XP_011515236.1:p.Ile675Thr
XM_011516935.1:c.1658T>C	XP_011515237.1:p.Ile553Thr
XM_011516936.1:c.1652T>C	XP_011515238.1:p.Ile551Thr
XM_011516937.1:c.2024T>C	XP_011515239.1:p.Ile675Thr
XM_011516938.1:c.1193T>C	XP_011515240.1:p.Ile398Thr
XM_011516939.1:c.722T>C	XP_011515241.1:p.Ile241Thr
XM_011516940.1:c.722T>C	XP_011515242.1:p.Ile241Thr
XM_011516941.1:c.2024T>C	XP_011515243.1:p.Ile675Thr
XM_011516942.1:c.2024T>C	XP_011515244.1:p.Ile675Thr
XR_242384.2:n.2154T>C
XR_928310.1:n.2154T>C
XR_928311.1:n.2154T>C
XR_928312.1:n.2154T>C
NM_001352890.2:c.2225T>C	NP_001339819.2:p.Ile742Thr
NM_001362798.1:c.2225T>C	NP_001349727.1:p.Ile742Thr
NM_014957.4:c.2024T>C	NP_055772.3:p.Ile675Thr
NR_148197.2:n.2321T>C
XM_005250840.5:c.2069T>C	XP_005250897.3:p.Ile690Thr
XM_005250841.4:c.2069T>C	XP_005250898.3:p.Ile690Thr
XM_005250842.4:c.1991T>C	XP_005250899.1:p.Ile664Thr
XM_011516933.2:c.2225T>C	XP_011515235.2:p.Ile742Thr
XM_011516934.3:c.2225T>C	XP_011515236.2:p.Ile742Thr
XM_011516937.2:c.2225T>C	XP_011515239.2:p.Ile742Thr
XM_011516938.3:c.1193T>C	XP_011515240.1:p.Ile398Thr
XM_011516939.3:c.722T>C	XP_011515241.1:p.Ile241Thr
XM_011516940.2:c.722T>C	XP_011515242.1:p.Ile241Thr
XM_011516941.3:c.2225T>C	XP_011515243.2:p.Ile742Thr
XM_017013241.1:c.2024T>C	XP_016868730.1:p.Ile675Thr
XM_017013242.1:c.1481T>C	XP_016868731.1:p.Ile494Thr
XM_017013243.1:c.761T>C	XP_016868732.1:p.Ile254Thr
XR_001745497.2:n.2371T>C
XR_001745498.2:n.2371T>C
XR_928310.3:n.2371T>C
XR_928312.3:n.2371T>C
NM_001352890.3:c.2225T>C MANE Select	NP_001339819.2:p.Ile742Thr
NM_001362798.2:c.2225T>C	NP_001349727.1:p.Ile742Thr
NM_014957.5:c.2024T>C	NP_055772.3:p.Ile675Thr
NR_148197.3:n.2344T>C