Canonical Allele Identifier: CA729786648

Gene: DENND1B

Linked Data

• dbSNP Id: rs1998598
• MyVariant Identifiers: chr1:g.197727642A>T (hg19) ; chr1:g.197758512A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000620048.6:c.82+14356T>A MANE Select	ENSP00000479816.1:n.82+14356T>A
ENST00000235453.8:c.-160+14356T>A	ENSP00000235453.4:n.-160+14356T>A
ENST00000294737.11:c.82+14356T>A	ENSP00000294737.7:n.82+14356T>A
ENST00000367396.7:c.82+14356T>A	ENSP00000356366.3:n.82+14356T>A
ENST00000422998.1:c.18+14356T>A	ENSP00000410025.1:n.18+14356T>A
ENST00000468589.5:n.353+14356T>A
ENST00000477581.1:n.410+14356T>A
ENST00000495550.5:n.186+14356T>A
ENST00000620048.4:c.82+14356T>A	ENSP00000479816.1:n.82+14356T>A
NM_001195215.1:c.82+14356T>A	NP_001182144.1:n.82+14356T>A
NM_001195216.1:c.82+14356T>A	NP_001182145.1:n.82+14356T>A
NM_001300858.1:c.-160+14356T>A	NP_001287787.1:n.-160+14356T>A
NM_144977.4:c.82+14356T>A	NP_659414.2:n.82+14356T>A
NR_125340.1:n.420+14356T>A
XM_005244931.2:c.82+14356T>A	XP_005244988.1:n.82+14356T>A
XM_006711192.2:c.-160+14356T>A	XP_006711255.1:n.-160+14356T>A
XM_006711193.2:c.-160+14356T>A	XP_006711256.1:n.-160+14356T>A
XM_011509246.1:c.226+14356T>A	XP_011507548.1:n.226+14356T>A
XM_011509247.1:c.226+14356T>A	XP_011507549.1:n.226+14356T>A
XM_011509248.1:c.121+14356T>A	XP_011507550.1:n.121+14356T>A
XM_011509249.1:c.-160+14356T>A	XP_011507551.1:n.-160+14356T>A
XM_011509250.1:c.-160+14356T>A	XP_011507552.1:n.-160+14356T>A
XM_011509251.1:c.226+14356T>A	XP_011507553.1:n.226+14356T>A
XM_006711193.3:c.-160+14356T>A	XP_006711256.1:n.-160+14356T>A
XM_011509246.2:c.226+14356T>A	XP_011507548.1:n.226+14356T>A
XM_011509248.2:c.121+14356T>A	XP_011507550.1:n.121+14356T>A
XM_011509249.2:c.-160+14356T>A	XP_011507551.1:n.-160+14356T>A
XM_011509251.3:c.226+14356T>A	XP_011507553.1:n.226+14356T>A
XM_017000470.1:c.-160+14356T>A	XP_016855959.1:n.-160+14356T>A
XM_017000471.1:c.-160+14356T>A	XP_016855960.1:n.-160+14356T>A
XM_024453626.1:c.-462+14356T>A	XP_024309394.1:n.-462+14356T>A
XM_024453627.1:c.-665+14356T>A	XP_024309395.1:n.-665+14356T>A
NM_001195215.2:c.82+14356T>A MANE Select	NP_001182144.1:n.82+14356T>A
NM_001195216.2:c.82+14356T>A	NP_001182145.1:n.82+14356T>A
NM_001300858.2:c.-160+14356T>A	NP_001287787.1:n.-160+14356T>A
NM_144977.5:c.82+14356T>A	NP_659414.2:n.82+14356T>A
NR_125340.2:n.407+14356T>A