Canonical Allele Identifier: CA476780238

Gene: ALG9

Linked Data

• MyVariant Identifiers: chr11:g.111706915G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111836192G>A , CM000673.2:g.111836192G>A	GRCh38
NC_000011.9:g.111706915G>A , CM000673.1:g.111706915G>A	GRCh37
NC_000011.8:g.111212125G>A	NCBI36
NG_009210.1:g.40390C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616540.5:c.1575C>T MANE Select	ENSP00000482437.1:p.Asp525=
ENST00000398006.6:c.1041C>T	ENSP00000381090.2:p.Asp347=
ENST00000526272.5:n.139C>T
ENST00000530851.6:n.537+17188C>T
ENST00000531154.5:c.1062C>T	ENSP00000435517.1:p.Asp354=
ENST00000532425.6:c.308C>T
ENST00000614444.4:c.1554C>T	ENSP00000484200.1:p.Asp518=
ENST00000616540.4:c.1575C>T	ENSP00000482437.1:p.Asp525=
ENST00000619129.4:c.*1106C>T	ENSP00000480661.1:n.*1106C>T
ENST00000622211.4:c.2253C>T	ENSP00000482396.1:p.Asp751=
NM_001077690.1:c.1554C>T	NP_001071158.1:p.Asp518=
NM_001077691.1:c.1062C>T	NP_001071159.1:p.Asp354=
NM_001077692.1:c.1041C>T	NP_001071160.1:p.Asp347=
NM_024740.2:c.1575C>T MANE Select	NP_079016.2:p.Asp525=
XM_005277723.3:c.1575C>T	XP_005277780.1:p.Asp525=
XM_005277724.3:c.1554C>T	XP_005277781.1:p.Asp518=
XM_006718913.2:c.1575C>T	XP_006718976.1:p.Asp525=
XM_011542990.1:c.1575C>T	XP_011541292.1:p.Asp525=
XM_011542991.1:c.1554C>T	XP_011541293.1:p.Asp518=
XM_011542992.1:c.1575C>T	XP_011541294.1:p.Asp525=
XM_011542993.1:c.1062C>T	XP_011541295.1:p.Asp354=
XM_011542994.1:c.1062C>T	XP_011541296.1:p.Asp354=
XM_011542995.1:c.1062C>T	XP_011541297.1:p.Asp354=
XM_011542996.1:c.1062C>T	XP_011541298.1:p.Asp354=
XM_011542997.1:c.987C>T	XP_011541299.1:p.Asp329=
XR_947863.1:n.1674C>T
XR_947864.1:n.1498C>T
XR_947865.1:n.1498C>T
NM_001352409.1:c.1041C>T	NP_001339338.1:p.Asp347=
NM_001352410.1:c.1041C>T	NP_001339339.1:p.Asp347=
NM_001352411.1:c.1041C>T	NP_001339340.1:p.Asp347=
NM_001352412.1:c.1041C>T	NP_001339341.1:p.Asp347=
NM_001352413.1:c.1062C>T	NP_001339342.1:p.Asp354=
NM_001352414.1:c.1062C>T	NP_001339343.1:p.Asp354=
NM_001352415.1:c.1041C>T	NP_001339344.1:p.Asp347=
NM_001352416.1:c.1041C>T	NP_001339345.1:p.Asp347=
NM_001352417.1:c.1554C>T	NP_001339346.1:p.Asp518=
NM_001352418.1:c.1431C>T	NP_001339347.1:p.Asp477=
NM_001352419.1:c.1062C>T	NP_001339348.1:p.Asp354=
NM_001352420.1:c.1041C>T	NP_001339349.1:p.Asp347=
NM_001352421.1:c.1041C>T	NP_001339350.1:p.Asp347=
NM_001352422.1:c.966C>T	NP_001339351.1:p.Asp322=
NM_001352423.1:c.918C>T	NP_001339352.1:p.Asp306=
NR_147984.1:n.1951C>T
XM_005277723.5:c.1575C>T	XP_005277780.1:p.Asp525=
XM_006718913.3:c.1575C>T	XP_006718976.1:p.Asp525=
XM_011542992.2:c.1575C>T	XP_011541294.1:p.Asp525=
XM_017018313.2:c.1554C>T	XP_016873802.1:p.Asp518=
XM_017018314.2:c.1452C>T	XP_016873803.1:p.Asp484=
XM_024448695.1:c.1554C>T	XP_024304463.1:p.Asp518=
XR_001747967.2:n.1663C>T
XR_001747968.2:n.1642C>T
XR_001747969.2:n.1540C>T
XR_001747970.2:n.1642C>T
XR_001747971.1:n.1971C>T
XR_001747972.1:n.1975C>T
XR_001747973.1:n.1678C>T
XR_001747974.1:n.1791C>T
XR_001747975.1:n.1950C>T
XR_001747976.1:n.1954C>T
XR_001747977.1:n.1127C>T
XR_001747979.1:n.1930C>T
XR_001747980.1:n.1626C>T
XR_947863.3:n.1663C>T
XR_947864.2:n.1487C>T
XR_947865.2:n.1487C>T
NM_001077691.2:c.1062C>T	NP_001071159.1:p.Asp354=
NM_001077692.2:c.1041C>T	NP_001071160.1:p.Asp347=
NM_001352411.2:c.1041C>T	NP_001339340.1:p.Asp347=
NM_001352412.2:c.1041C>T	NP_001339341.1:p.Asp347=
NM_001352414.2:c.1062C>T	NP_001339343.1:p.Asp354=
NM_001352420.2:c.1041C>T	NP_001339349.1:p.Asp347=
NM_001352421.2:c.1041C>T	NP_001339350.1:p.Asp347=
NM_001352422.2:c.966C>T	NP_001339351.1:p.Asp322=
NM_001352423.2:c.918C>T	NP_001339352.1:p.Asp306=
NR_147984.2:n.1971C>T