Canonical Allele Identifier: CA382591217
Gene: ALG9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111836170T>C , CM000673.2:g.111836170T>C GRCh38
NC_000011.9:g.111706893T>C , CM000673.1:g.111706893T>C GRCh37
NC_000011.8:g.111212103T>C NCBI36
NG_009210.1:g.40412A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000616540.5:c.1597A>G MANE Select ENSP00000482437.1:p.Arg533Gly
ENST00000398006.6:c.1063A>G ENSP00000381090.2:p.Arg355Gly
ENST00000526272.5:n.161A>G
ENST00000530851.6:n.537+17210A>G
ENST00000531154.5:c.1084A>G ENSP00000435517.1:p.Arg362Gly
ENST00000532425.6:c.330A>G
ENST00000614444.4:c.1576A>G ENSP00000484200.1:p.Arg526Gly
ENST00000616540.4:c.1597A>G ENSP00000482437.1:p.Arg533Gly
ENST00000619129.4:c.*1128A>G ENSP00000480661.1:n.*1128A>G
ENST00000622211.4:c.2275A>G ENSP00000482396.1:p.Arg759Gly
NM_001077690.1:c.1576A>G NP_001071158.1:p.Arg526Gly
NM_001077691.1:c.1084A>G NP_001071159.1:p.Arg362Gly
NM_001077692.1:c.1063A>G NP_001071160.1:p.Arg355Gly
NM_024740.2:c.1597A>G MANE Select NP_079016.2:p.Arg533Gly
XM_005277723.3:c.1597A>G XP_005277780.1:p.Arg533Gly
XM_005277724.3:c.1576A>G XP_005277781.1:p.Arg526Gly
XM_006718913.2:c.1597A>G XP_006718976.1:p.Arg533Gly
XM_011542990.1:c.1597A>G XP_011541292.1:p.Arg533Gly
XM_011542991.1:c.1576A>G XP_011541293.1:p.Arg526Gly
XM_011542992.1:c.1597A>G XP_011541294.1:p.Arg533Gly
XM_011542993.1:c.1084A>G XP_011541295.1:p.Arg362Gly
XM_011542994.1:c.1084A>G XP_011541296.1:p.Arg362Gly
XM_011542995.1:c.1084A>G XP_011541297.1:p.Arg362Gly
XM_011542996.1:c.1084A>G XP_011541298.1:p.Arg362Gly
XM_011542997.1:c.1009A>G XP_011541299.1:p.Arg337Gly
XR_947863.1:n.1696A>G
XR_947864.1:n.1520A>G
XR_947865.1:n.1520A>G
NM_001352409.1:c.1063A>G NP_001339338.1:p.Arg355Gly
NM_001352410.1:c.1063A>G NP_001339339.1:p.Arg355Gly
NM_001352411.1:c.1063A>G NP_001339340.1:p.Arg355Gly
NM_001352412.1:c.1063A>G NP_001339341.1:p.Arg355Gly
NM_001352413.1:c.1084A>G NP_001339342.1:p.Arg362Gly
NM_001352414.1:c.1084A>G NP_001339343.1:p.Arg362Gly
NM_001352415.1:c.1063A>G NP_001339344.1:p.Arg355Gly
NM_001352416.1:c.1063A>G NP_001339345.1:p.Arg355Gly
NM_001352417.1:c.1576A>G NP_001339346.1:p.Arg526Gly
NM_001352418.1:c.1453A>G NP_001339347.1:p.Arg485Gly
NM_001352419.1:c.1084A>G NP_001339348.1:p.Arg362Gly
NM_001352420.1:c.1063A>G NP_001339349.1:p.Arg355Gly
NM_001352421.1:c.1063A>G NP_001339350.1:p.Arg355Gly
NM_001352422.1:c.988A>G NP_001339351.1:p.Arg330Gly
NM_001352423.1:c.940A>G NP_001339352.1:p.Arg314Gly
NR_147984.1:n.1973A>G
XM_005277723.5:c.1597A>G XP_005277780.1:p.Arg533Gly
XM_006718913.3:c.1597A>G XP_006718976.1:p.Arg533Gly
XM_011542992.2:c.1597A>G XP_011541294.1:p.Arg533Gly
XM_017018313.2:c.1576A>G XP_016873802.1:p.Arg526Gly
XM_017018314.2:c.1474A>G XP_016873803.1:p.Arg492Gly
XM_024448695.1:c.1576A>G XP_024304463.1:p.Arg526Gly
XR_001747967.2:n.1685A>G
XR_001747968.2:n.1664A>G
XR_001747969.2:n.1562A>G
XR_001747970.2:n.1664A>G
XR_001747971.1:n.1993A>G
XR_001747972.1:n.1997A>G
XR_001747973.1:n.1700A>G
XR_001747974.1:n.1813A>G
XR_001747975.1:n.1972A>G
XR_001747976.1:n.1976A>G
XR_001747977.1:n.1149A>G
XR_001747979.1:n.1952A>G
XR_001747980.1:n.1648A>G
XR_947863.3:n.1685A>G
XR_947864.2:n.1509A>G
XR_947865.2:n.1509A>G
NM_001077691.2:c.1084A>G NP_001071159.1:p.Arg362Gly
NM_001077692.2:c.1063A>G NP_001071160.1:p.Arg355Gly
NM_001352411.2:c.1063A>G NP_001339340.1:p.Arg355Gly
NM_001352412.2:c.1063A>G NP_001339341.1:p.Arg355Gly
NM_001352414.2:c.1084A>G NP_001339343.1:p.Arg362Gly
NM_001352420.2:c.1063A>G NP_001339349.1:p.Arg355Gly
NM_001352421.2:c.1063A>G NP_001339350.1:p.Arg355Gly
NM_001352422.2:c.988A>G NP_001339351.1:p.Arg330Gly
NM_001352423.2:c.940A>G NP_001339352.1:p.Arg314Gly
NR_147984.2:n.1993A>G