Canonical Allele Identifier: CA228538218
Community Standard Title: NM_024740.2(ALG9):c.*1297A>G
Gene: ALG9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111785100T>C , CM000673.2:g.111785100T>C GRCh38
NC_000011.9:g.111655824T>C , CM000673.1:g.111655824T>C GRCh37
NC_000011.8:g.111161034T>C NCBI36
NG_009210.1:g.91481A>G

Transcript Alleles

HGVS Amino-acid Change
NM_024740.2:c.*1297A>G MANE Select NP_079016.2:n.*1297A>G
ENST00000616540.5:c.*1297A>G MANE Select ENSP00000482437.1:n.*1297A>G
NM_001077690.1:c.*1297A>G NP_001071158.1:n.*1297A>G
NM_001077691.1:c.*1297A>G NP_001071159.1:n.*1297A>G
NM_001077691.2:c.*1297A>G NP_001071159.1:n.*1297A>G
NM_001077692.1:c.*1297A>G NP_001071160.1:n.*1297A>G
NM_001077692.2:c.*1297A>G NP_001071160.1:n.*1297A>G
NM_001352409.1:c.*1297A>G NP_001339338.1:n.*1297A>G
NM_001352410.1:c.*1297A>G NP_001339339.1:n.*1297A>G
NM_001352411.1:c.*1297A>G NP_001339340.1:n.*1297A>G
NM_001352411.2:c.*1297A>G NP_001339340.1:n.*1297A>G
NM_001352412.1:c.*1297A>G NP_001339341.1:n.*1297A>G
NM_001352412.2:c.*1297A>G NP_001339341.1:n.*1297A>G
NM_001352413.1:c.*1297A>G NP_001339342.1:n.*1297A>G
NM_001352414.1:c.*1297A>G NP_001339343.1:n.*1297A>G
NM_001352414.2:c.*1297A>G NP_001339343.1:n.*1297A>G
NM_001352415.1:c.*957A>G NP_001339344.1:n.*957A>G
NM_001352416.1:c.*957A>G NP_001339345.1:n.*957A>G
NM_001352417.1:c.*957A>G NP_001339346.1:n.*957A>G
NM_001352418.1:c.*1297A>G NP_001339347.1:n.*1297A>G
NM_001352419.1:c.*957A>G NP_001339348.1:n.*957A>G
NM_001352420.1:c.*1426A>G NP_001339349.1:n.*1426A>G
NM_001352420.2:c.*1426A>G NP_001339349.1:n.*1426A>G
NM_001352421.1:c.*1420A>G NP_001339350.1:n.*1420A>G
NM_001352421.2:c.*1420A>G NP_001339350.1:n.*1420A>G
NM_001352422.1:c.*1297A>G NP_001339351.1:n.*1297A>G
NM_001352422.2:c.*1297A>G NP_001339351.1:n.*1297A>G
NM_001352423.1:c.*1297A>G NP_001339352.1:n.*1297A>G
NM_001352423.2:c.*1297A>G NP_001339352.1:n.*1297A>G
NR_147984.1:n.3752A>G
NR_147984.2:n.3772A>G
ENST00000532425.6:c.1580A>G
XM_005277723.3:c.*957A>G XP_005277780.1:n.*957A>G
XM_005277723.5:c.*957A>G XP_005277780.1:n.*957A>G
XM_005277724.3:c.*957A>G XP_005277781.1:n.*957A>G
XM_017018314.2:c.*1297A>G XP_016873803.1:n.*1297A>G
XR_001747967.2:n.2246+689A>G
XR_001747968.2:n.2225+689A>G
XR_001747969.2:n.2123+689A>G
XR_001747971.1:n.2554+689A>G
XR_001747972.1:n.2558+689A>G
XR_001747973.1:n.2261+689A>G
XR_001747974.1:n.2374+689A>G
XR_001747975.1:n.2533+689A>G
XR_001747976.1:n.2537+689A>G
XR_001747977.1:n.1710+689A>G