Canonical Allele Identifier: CA2480658762

Gene: DENND4B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153941294A>C , CM000663.2:g.153941294A>C	GRCh38
NC_000001.10:g.153913770A>C , CM000663.1:g.153913770A>C	GRCh37
NC_000001.9:g.152180394A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361217.9:c.1123-5T>G MANE Select	ENSP00000354597.4:n.1123-5T>G
ENST00000361217.8:c.1123-5T>G	ENSP00000354597.4:n.1123-5T>G
ENST00000368646.6:c.1156-5T>G	ENSP00000357635.2:n.1156-5T>G
ENST00000483561.2:n.444-5T>G
ENST00000494683.1:n.62-5T>G
NM_014856.2:c.1123-5T>G	NP_055671.2:n.1123-5T>G
XM_005245678.3:c.1156-5T>G	XP_005245735.1:n.1156-5T>G
XM_005245679.2:c.1123-5T>G	XP_005245736.1:n.1123-5T>G
XM_011510219.1:c.1123-5T>G	XP_011508521.1:n.1123-5T>G
XM_011510220.1:c.808-5T>G	XP_011508522.1:n.808-5T>G
XM_011510221.1:c.517-5T>G	XP_011508523.1:n.517-5T>G
XM_011510222.1:c.1123-5T>G	XP_011508524.1:n.1123-5T>G
XR_426806.2:n.1146-5T>G
XM_005245678.4:c.1156-5T>G	XP_005245735.1:n.1156-5T>G
XM_011510220.2:c.808-5T>G	XP_011508522.1:n.808-5T>G
XM_011510221.3:c.517-5T>G	XP_011508523.1:n.517-5T>G
NM_001367466.1:c.1156-5T>G	NP_001354395.1:n.1156-5T>G
NM_014856.3:c.1123-5T>G MANE Select	NP_055671.2:n.1123-5T>G