Canonical Allele Identifier: CA9126823
Gene: DENND1C HGNC NCBI

Linked Data

dbSNP Id: rs3745571
ExAC: 19:6475613 T / C
gnomAD v2: 19-6475613-T-C
gnomAD v3: 19-6475602-T-C
gnomAD v4: 19-6475602-T-C
MyVariant Identifiers: chr19:g.6475613T>C (hg19) chr19:g.6475602T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6475602T>C , CM000681.2:g.6475602T>C GRCh38
NC_000019.9:g.6475613T>C , CM000681.1:g.6475613T>C GRCh37
NC_000019.8:g.6426613T>C NCBI36
NG_054762.1:g.11207A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381480.7:c.826-17A>G MANE Select ENSP00000370889.1:n.826-17A>G
ENST00000381480.6:c.826-17A>G ENSP00000370889.1:n.826-17A>G
ENST00000543576.5:c.694-17A>G ENSP00000437805.1:n.694-17A>G
ENST00000590444.5:n.452A>G
ENST00000590818.5:n.529A>G
ENST00000590867.5:c.*41A>G ENSP00000465675.1:n.*41A>G
NM_001290331.1:c.694-17A>G NP_001277260.1:n.694-17A>G
NM_024898.3:c.826-17A>G NP_079174.2:n.826-17A>G
XM_006722905.2:c.694-17A>G XP_006722968.2:n.694-17A>G
XM_006722906.2:c.694-17A>G XP_006722969.1:n.694-17A>G
XM_011528318.1:c.694-17A>G XP_011526620.1:n.694-17A>G
XM_006722905.3:c.1237-17A>G XP_006722968.3:n.1237-17A>G
XM_006722906.3:c.694-17A>G XP_006722969.1:n.694-17A>G
XM_011528318.2:c.694-17A>G XP_011526620.1:n.694-17A>G
XM_024451727.1:c.1237-17A>G XP_024307495.1:n.1237-17A>G
NM_024898.4:c.826-17A>G MANE Select NP_079174.2:n.826-17A>G
NM_001290331.2:c.694-17A>G NP_001277260.1:n.694-17A>G
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