Canonical Allele Identifier: CA1218207100
Gene: DENND1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197763981A= , CM000663.2:g.197763981A= GRCh38
NC_000001.10:g.197733111A= , CM000663.1:g.197733111A= GRCh37
NC_000001.9:g.195999734A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000620048.6:c.82+8887T= MANE Select ENSP00000479816.1:n.82+8887T=
ENST00000235453.8:c.-160+8887T= ENSP00000235453.4:n.-160+8887T=
ENST00000294737.11:c.82+8887T= ENSP00000294737.7:n.82+8887T=
ENST00000367396.7:c.82+8887T= ENSP00000356366.3:n.82+8887T=
ENST00000422998.1:c.18+8887T= ENSP00000410025.1:n.18+8887T=
ENST00000468589.5:n.353+8887T=
ENST00000477581.1:n.410+8887T=
ENST00000495550.5:n.186+8887T=
ENST00000620048.4:c.82+8887T= ENSP00000479816.1:n.82+8887T=
NM_001195215.1:c.82+8887T= NP_001182144.1:n.82+8887T=
NM_001195216.1:c.82+8887T= NP_001182145.1:n.82+8887T=
NM_001300858.1:c.-160+8887T= NP_001287787.1:n.-160+8887T=
NM_144977.4:c.82+8887T= NP_659414.2:n.82+8887T=
NR_125340.1:n.420+8887T=
XM_005244931.2:c.82+8887T= XP_005244988.1:n.82+8887T=
XM_006711192.2:c.-160+8887T= XP_006711255.1:n.-160+8887T=
XM_006711193.2:c.-160+8887T= XP_006711256.1:n.-160+8887T=
XM_011509246.1:c.226+8887T= XP_011507548.1:n.226+8887T=
XM_011509247.1:c.226+8887T= XP_011507549.1:n.226+8887T=
XM_011509248.1:c.121+8887T= XP_011507550.1:n.121+8887T=
XM_011509249.1:c.-160+8887T= XP_011507551.1:n.-160+8887T=
XM_011509250.1:c.-160+8887T= XP_011507552.1:n.-160+8887T=
XM_011509251.1:c.226+8887T= XP_011507553.1:n.226+8887T=
XM_006711193.3:c.-160+8887T= XP_006711256.1:n.-160+8887T=
XM_011509246.2:c.226+8887T= XP_011507548.1:n.226+8887T=
XM_011509248.2:c.121+8887T= XP_011507550.1:n.121+8887T=
XM_011509249.2:c.-160+8887T= XP_011507551.1:n.-160+8887T=
XM_011509251.3:c.226+8887T= XP_011507553.1:n.226+8887T=
XM_017000470.1:c.-160+8887T= XP_016855959.1:n.-160+8887T=
XM_017000471.1:c.-160+8887T= XP_016855960.1:n.-160+8887T=
XM_024453626.1:c.-462+8887T= XP_024309394.1:n.-462+8887T=
XM_024453627.1:c.-665+8887T= XP_024309395.1:n.-665+8887T=
NM_001195215.2:c.82+8887T= MANE Select NP_001182144.1:n.82+8887T=
NM_001195216.2:c.82+8887T= NP_001182145.1:n.82+8887T=
NM_001300858.2:c.-160+8887T= NP_001287787.1:n.-160+8887T=
NM_144977.5:c.82+8887T= NP_659414.2:n.82+8887T=
NR_125340.2:n.407+8887T=