Canonical Allele Identifier: CA476780211
Gene: ALG9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.111706900C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111836177C>T , CM000673.2:g.111836177C>T GRCh38
NC_000011.9:g.111706900C>T , CM000673.1:g.111706900C>T GRCh37
NC_000011.8:g.111212110C>T NCBI36
NG_009210.1:g.40405G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000616540.5:c.1590G>A MANE Select ENSP00000482437.1:p.Glu530=
ENST00000398006.6:c.1056G>A ENSP00000381090.2:p.Glu352=
ENST00000526272.5:n.154G>A
ENST00000530851.6:n.537+17203G>A
ENST00000531154.5:c.1077G>A ENSP00000435517.1:p.Glu359=
ENST00000532425.6:c.323G>A
ENST00000614444.4:c.1569G>A ENSP00000484200.1:p.Glu523=
ENST00000616540.4:c.1590G>A ENSP00000482437.1:p.Glu530=
ENST00000619129.4:c.*1121G>A ENSP00000480661.1:n.*1121G>A
ENST00000622211.4:c.2268G>A ENSP00000482396.1:p.Glu756=
NM_001077690.1:c.1569G>A NP_001071158.1:p.Glu523=
NM_001077691.1:c.1077G>A NP_001071159.1:p.Glu359=
NM_001077692.1:c.1056G>A NP_001071160.1:p.Glu352=
NM_024740.2:c.1590G>A MANE Select NP_079016.2:p.Glu530=
XM_005277723.3:c.1590G>A XP_005277780.1:p.Glu530=
XM_005277724.3:c.1569G>A XP_005277781.1:p.Glu523=
XM_006718913.2:c.1590G>A XP_006718976.1:p.Glu530=
XM_011542990.1:c.1590G>A XP_011541292.1:p.Glu530=
XM_011542991.1:c.1569G>A XP_011541293.1:p.Glu523=
XM_011542992.1:c.1590G>A XP_011541294.1:p.Glu530=
XM_011542993.1:c.1077G>A XP_011541295.1:p.Glu359=
XM_011542994.1:c.1077G>A XP_011541296.1:p.Glu359=
XM_011542995.1:c.1077G>A XP_011541297.1:p.Glu359=
XM_011542996.1:c.1077G>A XP_011541298.1:p.Glu359=
XM_011542997.1:c.1002G>A XP_011541299.1:p.Glu334=
XR_947863.1:n.1689G>A
XR_947864.1:n.1513G>A
XR_947865.1:n.1513G>A
NM_001352409.1:c.1056G>A NP_001339338.1:p.Glu352=
NM_001352410.1:c.1056G>A NP_001339339.1:p.Glu352=
NM_001352411.1:c.1056G>A NP_001339340.1:p.Glu352=
NM_001352412.1:c.1056G>A NP_001339341.1:p.Glu352=
NM_001352413.1:c.1077G>A NP_001339342.1:p.Glu359=
NM_001352414.1:c.1077G>A NP_001339343.1:p.Glu359=
NM_001352415.1:c.1056G>A NP_001339344.1:p.Glu352=
NM_001352416.1:c.1056G>A NP_001339345.1:p.Glu352=
NM_001352417.1:c.1569G>A NP_001339346.1:p.Glu523=
NM_001352418.1:c.1446G>A NP_001339347.1:p.Glu482=
NM_001352419.1:c.1077G>A NP_001339348.1:p.Glu359=
NM_001352420.1:c.1056G>A NP_001339349.1:p.Glu352=
NM_001352421.1:c.1056G>A NP_001339350.1:p.Glu352=
NM_001352422.1:c.981G>A NP_001339351.1:p.Glu327=
NM_001352423.1:c.933G>A NP_001339352.1:p.Glu311=
NR_147984.1:n.1966G>A
XM_005277723.5:c.1590G>A XP_005277780.1:p.Glu530=
XM_006718913.3:c.1590G>A XP_006718976.1:p.Glu530=
XM_011542992.2:c.1590G>A XP_011541294.1:p.Glu530=
XM_017018313.2:c.1569G>A XP_016873802.1:p.Glu523=
XM_017018314.2:c.1467G>A XP_016873803.1:p.Glu489=
XM_024448695.1:c.1569G>A XP_024304463.1:p.Glu523=
XR_001747967.2:n.1678G>A
XR_001747968.2:n.1657G>A
XR_001747969.2:n.1555G>A
XR_001747970.2:n.1657G>A
XR_001747971.1:n.1986G>A
XR_001747972.1:n.1990G>A
XR_001747973.1:n.1693G>A
XR_001747974.1:n.1806G>A
XR_001747975.1:n.1965G>A
XR_001747976.1:n.1969G>A
XR_001747977.1:n.1142G>A
XR_001747979.1:n.1945G>A
XR_001747980.1:n.1641G>A
XR_947863.3:n.1678G>A
XR_947864.2:n.1502G>A
XR_947865.2:n.1502G>A
NM_001077691.2:c.1077G>A NP_001071159.1:p.Glu359=
NM_001077692.2:c.1056G>A NP_001071160.1:p.Glu352=
NM_001352411.2:c.1056G>A NP_001339340.1:p.Glu352=
NM_001352412.2:c.1056G>A NP_001339341.1:p.Glu352=
NM_001352414.2:c.1077G>A NP_001339343.1:p.Glu359=
NM_001352420.2:c.1056G>A NP_001339349.1:p.Glu352=
NM_001352421.2:c.1056G>A NP_001339350.1:p.Glu352=
NM_001352422.2:c.981G>A NP_001339351.1:p.Glu327=
NM_001352423.2:c.933G>A NP_001339352.1:p.Glu311=
NR_147984.2:n.1986G>A