Canonical Allele Identifier: CA16075767
Gene: DENND1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1998598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197758512A>G , CM000663.2:g.197758512A>G GRCh38
NC_000001.9:g.195994265A>G NCBI36
NC_000001.10:g.197727642A>G , CM000663.1:g.197727642A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000235453.8:c.-160+14356T>C ENSP00000235453.4:p.=
ENST00000294737.11:c.82+14356T>C ENSP00000294737.7:p.=
ENST00000367396.7:c.82+14356T>C ENSP00000356366.3:p.=
ENST00000422998.1:c.18+14356T>C ENSP00000410025.1:p.=
ENST00000468589.5:n.353+14356T>C
ENST00000477581.1:n.410+14356T>C
ENST00000495550.5:n.186+14356T>C
ENST00000620048.4:c.82+14356T>C ENSP00000479816.1:p.=
NM_001195215.1:c.82+14356T>C VV NP_001182144.1:p.=
NM_001195216.1:c.82+14356T>C VV NP_001182145.1:p.=
NM_001300858.1:c.-160+14356T>C VV NP_001287787.1:p.=
NM_144977.4:c.82+14356T>C VV NP_659414.2:p.=
NR_125340.1:n.420+14356T>C
XM_005244931.2:c.82+14356T>C XP_005244988.1:p.=
XM_006711192.2:c.-160+14356T>C XP_006711255.1:p.=
XM_006711193.2:c.-160+14356T>C XP_006711256.1:p.=
XM_011509246.1:c.226+14356T>C XP_011507548.1:p.=
XM_011509247.1:c.226+14356T>C XP_011507549.1:p.=
XM_011509248.1:c.121+14356T>C XP_011507550.1:p.=
XM_011509249.1:c.-160+14356T>C XP_011507551.1:p.=
XM_011509250.1:c.-160+14356T>C XP_011507552.1:p.=
XM_011509251.1:c.226+14356T>C XP_011507553.1:p.=
XM_006711193.3:c.-160+14356T>C
XM_011509246.2:c.226+14356T>C
XM_011509248.2:c.121+14356T>C
XM_011509249.2:c.-160+14356T>C
XM_011509251.3:c.226+14356T>C
XM_017000470.1:c.-160+14356T>C XP_016855959.1:p.=
XM_017000471.1:c.-160+14356T>C XP_016855960.1:p.=
XM_024453626.1:c.-462+14356T>C XP_024309394.1:p.=
XM_024453627.1:c.-665+14356T>C XP_024309395.1:p.=