Canonical Allele Identifier: CA2000443650

Gene: ALG9

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111836140A= , CM000673.2:g.111836140A=	GRCh38
NC_000011.9:g.111706863A= , CM000673.1:g.111706863A=	GRCh37
NC_000011.8:g.111212073A=	NCBI36
NG_009210.1:g.40442T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616540.5:c.1602+25T= MANE Select	ENSP00000482437.1:n.1602+25T=
ENST00000398006.6:c.1068+25T=	ENSP00000381090.2:n.1068+25T=
ENST00000526272.5:n.166+25T=
ENST00000530851.6:n.537+17240T=
ENST00000531154.5:c.1089+25T=	ENSP00000435517.1:n.1089+25T=
ENST00000532425.6:c.335+25T=
ENST00000614444.4:c.1581+25T=	ENSP00000484200.1:n.1581+25T=
ENST00000616540.4:c.1602+25T=	ENSP00000482437.1:n.1602+25T=
ENST00000619129.4:c.*1133+25T=	ENSP00000480661.1:n.*1133+25T=
ENST00000622211.4:c.2280+25T=	ENSP00000482396.1:n.2280+25T=
NM_001077690.1:c.1581+25T=	NP_001071158.1:n.1581+25T=
NM_001077691.1:c.1089+25T=	NP_001071159.1:n.1089+25T=
NM_001077692.1:c.1068+25T=	NP_001071160.1:n.1068+25T=
NM_024740.2:c.1602+25T= MANE Select	NP_079016.2:n.1602+25T=
XM_005277723.3:c.1602+25T=	XP_005277780.1:n.1602+25T=
XM_005277724.3:c.1581+25T=	XP_005277781.1:n.1581+25T=
XM_006718913.2:c.1602+25T=	XP_006718976.1:n.1602+25T=
XM_011542990.1:c.1602+25T=	XP_011541292.1:n.1602+25T=
XM_011542991.1:c.1581+25T=	XP_011541293.1:n.1581+25T=
XM_011542992.1:c.1602+25T=	XP_011541294.1:n.1602+25T=
XM_011542993.1:c.1089+25T=	XP_011541295.1:n.1089+25T=
XM_011542994.1:c.1089+25T=	XP_011541296.1:n.1089+25T=
XM_011542995.1:c.1089+25T=	XP_011541297.1:n.1089+25T=
XM_011542996.1:c.1089+25T=	XP_011541298.1:n.1089+25T=
XM_011542997.1:c.1014+25T=	XP_011541299.1:n.1014+25T=
XR_947863.1:n.1701+25T=
XR_947864.1:n.1525+25T=
XR_947865.1:n.1525+25T=
NM_001352409.1:c.1068+25T=	NP_001339338.1:n.1068+25T=
NM_001352410.1:c.1068+25T=	NP_001339339.1:n.1068+25T=
NM_001352411.1:c.1068+25T=	NP_001339340.1:n.1068+25T=
NM_001352412.1:c.1068+25T=	NP_001339341.1:n.1068+25T=
NM_001352413.1:c.1089+25T=	NP_001339342.1:n.1089+25T=
NM_001352414.1:c.1089+25T=	NP_001339343.1:n.1089+25T=
NM_001352415.1:c.1068+25T=	NP_001339344.1:n.1068+25T=
NM_001352416.1:c.1068+25T=	NP_001339345.1:n.1068+25T=
NM_001352417.1:c.1581+25T=	NP_001339346.1:n.1581+25T=
NM_001352418.1:c.1458+25T=	NP_001339347.1:n.1458+25T=
NM_001352419.1:c.1089+25T=	NP_001339348.1:n.1089+25T=
NM_001352420.1:c.1068+25T=	NP_001339349.1:n.1068+25T=
NM_001352421.1:c.1068+25T=	NP_001339350.1:n.1068+25T=
NM_001352422.1:c.993+25T=	NP_001339351.1:n.993+25T=
NM_001352423.1:c.945+25T=	NP_001339352.1:n.945+25T=
NR_147984.1:n.1978+25T=
XM_005277723.5:c.1602+25T=	XP_005277780.1:n.1602+25T=
XM_006718913.3:c.1602+25T=	XP_006718976.1:n.1602+25T=
XM_011542992.2:c.1602+25T=	XP_011541294.1:n.1602+25T=
XM_017018313.2:c.1581+25T=	XP_016873802.1:n.1581+25T=
XM_017018314.2:c.1479+25T=	XP_016873803.1:n.1479+25T=
XM_024448695.1:c.1581+25T=	XP_024304463.1:n.1581+25T=
XR_001747967.2:n.1690+25T=
XR_001747968.2:n.1669+25T=
XR_001747969.2:n.1567+25T=
XR_001747970.2:n.1669+25T=
XR_001747971.1:n.1998+25T=
XR_001747972.1:n.2002+25T=
XR_001747973.1:n.1705+25T=
XR_001747974.1:n.1818+25T=
XR_001747975.1:n.1977+25T=
XR_001747976.1:n.1981+25T=
XR_001747977.1:n.1154+25T=
XR_001747979.1:n.1957+25T=
XR_001747980.1:n.1653+25T=
XR_947863.3:n.1690+25T=
XR_947864.2:n.1514+25T=
XR_947865.2:n.1514+25T=
NM_001077691.2:c.1089+25T=	NP_001071159.1:n.1089+25T=
NM_001077692.2:c.1068+25T=	NP_001071160.1:n.1068+25T=
NM_001352411.2:c.1068+25T=	NP_001339340.1:n.1068+25T=
NM_001352412.2:c.1068+25T=	NP_001339341.1:n.1068+25T=
NM_001352414.2:c.1089+25T=	NP_001339343.1:n.1089+25T=
NM_001352420.2:c.1068+25T=	NP_001339349.1:n.1068+25T=
NM_001352421.2:c.1068+25T=	NP_001339350.1:n.1068+25T=
NM_001352422.2:c.993+25T=	NP_001339351.1:n.993+25T=
NM_001352423.2:c.945+25T=	NP_001339352.1:n.945+25T=
NR_147984.2:n.1998+25T=