Canonical Allele Identifier: CA1878122359

Gene: DENND1A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123787924_123787925delinsAT , CM000671.2:g.123787924_123787925delinsAT	GRCh38
NC_000009.11:g.126550203_126550204delinsAT , CM000671.1:g.126550203_126550204delinsAT	GRCh37
NC_000009.10:g.125590024_125590025delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394215.7:c.132+4662_132+4663delinsAT MANE Select	ENSP00000377763.4:n.132+4662_132+4663delinsAT
ENST00000373618.1:c.86+4662_86+4663delinsAT	ENSP00000362720.1:n.86+4662_86+4663delinsAT
ENST00000373620.7:c.132+4662_132+4663delinsAT	ENSP00000362722.3:n.132+4662_132+4663delinsAT
ENST00000373624.6:c.132+4662_132+4663delinsAT	ENSP00000362727.2:n.132+4662_132+4663delinsAT
ENST00000473039.5:n.299+4662_299+4663delinsAT
NM_020946.1:c.132+4662_132+4663delinsAT	NP_065997.1:n.132+4662_132+4663delinsAT
NM_024820.2:c.132+4662_132+4663delinsAT	NP_079096.2:n.132+4662_132+4663delinsAT
XM_005252109.2:c.132+4662_132+4663delinsAT	XP_005252166.1:n.132+4662_132+4663delinsAT
XM_005252111.3:c.177+4662_177+4663delinsAT	XP_005252168.1:n.177+4662_177+4663delinsAT
XM_005252113.3:c.177+4662_177+4663delinsAT	XP_005252170.1:n.177+4662_177+4663delinsAT
XM_006717195.2:c.177+4662_177+4663delinsAT	XP_006717258.1:n.177+4662_177+4663delinsAT
XM_011518882.1:c.177+4662_177+4663delinsAT	XP_011517184.1:n.177+4662_177+4663delinsAT
XM_011518883.1:c.177+4662_177+4663delinsAT	XP_011517185.1:n.177+4662_177+4663delinsAT
XM_011518884.1:c.140+4662_140+4663delinsAT	XP_011517186.1:n.140+4662_140+4663delinsAT
XM_011518885.1:c.69+4662_69+4663delinsAT	XP_011517187.1:n.69+4662_69+4663delinsAT
XM_011518886.1:c.177+4662_177+4663delinsAT	XP_011517188.1:n.177+4662_177+4663delinsAT
XM_011518887.1:c.177+4662_177+4663delinsAT	XP_011517189.1:n.177+4662_177+4663delinsAT
XR_929829.1:n.1165+4662_1165+4663delinsAT
XR_929830.1:n.1162+4662_1162+4663delinsAT
NM_001352964.1:c.132+4662_132+4663delinsAT	NP_001339893.1:n.132+4662_132+4663delinsAT
NM_001352965.1:c.37-18362_37-18361delinsAT	NP_001339894.1:n.37-18362_37-18361delinsAT
NM_001352966.1:c.43-18362_43-18361delinsAT	NP_001339895.1:n.43-18362_43-18361delinsAT
NM_001352967.1:c.86+4662_86+4663delinsAT	NP_001339896.1:n.86+4662_86+4663delinsAT
NM_001352968.1:c.86+4662_86+4663delinsAT	NP_001339897.1:n.86+4662_86+4663delinsAT
NR_148208.1:n.365+4662_365+4663delinsAT
XM_005252111.4:c.177+4662_177+4663delinsAT	XP_005252168.1:n.177+4662_177+4663delinsAT
XM_005252113.5:c.177+4662_177+4663delinsAT	XP_005252170.1:n.177+4662_177+4663delinsAT
XM_006717195.4:c.177+4662_177+4663delinsAT	XP_006717258.1:n.177+4662_177+4663delinsAT
XM_011518882.3:c.177+4662_177+4663delinsAT	XP_011517184.1:n.177+4662_177+4663delinsAT
XM_011518883.3:c.177+4662_177+4663delinsAT	XP_011517185.1:n.177+4662_177+4663delinsAT
XM_011518885.3:c.69+4662_69+4663delinsAT	XP_011517187.1:n.69+4662_69+4663delinsAT
XM_011518886.3:c.177+4662_177+4663delinsAT	XP_011517188.1:n.177+4662_177+4663delinsAT
XM_011518887.3:c.177+4662_177+4663delinsAT	XP_011517189.1:n.177+4662_177+4663delinsAT
XM_017014948.2:c.132+4662_132+4663delinsAT	XP_016870437.1:n.132+4662_132+4663delinsAT
XM_017014949.2:c.177+4662_177+4663delinsAT	XP_016870438.1:n.177+4662_177+4663delinsAT
XM_017014950.2:c.177+4662_177+4663delinsAT	XP_016870439.1:n.177+4662_177+4663delinsAT
XM_017014951.2:c.86+4662_86+4663delinsAT	XP_016870440.1:n.86+4662_86+4663delinsAT
XM_017014952.2:c.-599-18362_-599-18361delinsAT	XP_016870441.1:n.-599-18362_-599-18361delinsAT
XM_024447621.1:c.86+4662_86+4663delinsAT	XP_024303389.1:n.86+4662_86+4663delinsAT
XM_024447622.1:c.43-18362_43-18361delinsAT	XP_024303390.1:n.43-18362_43-18361delinsAT
XM_024447624.1:c.177+4662_177+4663delinsAT	XP_024303392.1:n.177+4662_177+4663delinsAT
XR_929829.2:n.1174+4662_1174+4663delinsAT
XR_929830.3:n.1171+4662_1171+4663delinsAT
NM_001352966.2:c.43-18362_43-18361delinsAT	NP_001339895.1:n.43-18362_43-18361delinsAT
NM_001352967.2:c.86+4662_86+4663delinsAT	NP_001339896.1:n.86+4662_86+4663delinsAT
NM_001352968.2:c.86+4662_86+4663delinsAT	NP_001339897.1:n.86+4662_86+4663delinsAT
NM_024820.3:c.132+4662_132+4663delinsAT	NP_079096.2:n.132+4662_132+4663delinsAT
NR_148208.2:n.353+4662_353+4663delinsAT
NM_001352964.2:c.132+4662_132+4663delinsAT MANE Select	NP_001339893.1:n.132+4662_132+4663delinsAT
NM_001352965.2:c.37-18362_37-18361delinsAT	NP_001339894.1:n.37-18362_37-18361delinsAT
NM_001393654.1:c.132+4662_132+4663delinsAT	NP_001380583.1:n.132+4662_132+4663delinsAT
NM_020946.2:c.132+4662_132+4663delinsAT	NP_065997.1:n.132+4662_132+4663delinsAT
NM_001400446.1:c.43-18362_43-18361delinsAT	NP_001387375.1:n.43-18362_43-18361delinsAT
NM_001400449.1:c.86+4662_86+4663delinsAT	NP_001387378.1:n.86+4662_86+4663delinsAT