Canonical Allele Identifier: CA394673939

Gene: ALG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5082649C>T , CM000678.2:g.5082649C>T	GRCh38
NC_000016.9:g.5132650C>T , CM000678.1:g.5132650C>T	GRCh37
NC_000016.8:g.5072651C>T	NCBI36
NG_009202.1:g.15841C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_019109.5:c.1163C>T MANE Select	NP_061982.3:p.Pro388Leu
ENST00000262374.10:c.1163C>T MANE Select	ENSP00000262374.5:p.Pro388Leu
NM_001330504.1:c.830C>T	NP_001317433.1:p.Pro277Leu
NM_001330504.2:c.830C>T	NP_001317433.1:p.Pro277Leu
NM_019109.4:c.1163C>T	NP_061982.3:p.Pro388Leu
ENST00000262374.9:c.1163C>T	ENSP00000262374.4:p.Pro388Leu
ENST00000544428.1:c.830C>T	ENSP00000440019.1:p.Pro277Leu
ENST00000588623.5:c.830C>T	ENSP00000468118.1:p.Pro277Leu
ENST00000591822.5:c.*1064C>T	ENSP00000467865.1:n.*1064C>T
ENST00000592793.6:n.3299C>T
ENST00000650085.1:n.1987C>T
ENST00000682020.1:c.569C>T	ENSP00000508075.1:p.Pro190Leu
ENST00000682206.1:c.*258C>T	ENSP00000508285.1:n.*258C>T
ENST00000682314.1:n.1211C>T
ENST00000682327.1:c.635C>T	ENSP00000507058.1:p.Pro212Leu
ENST00000682349.1:n.3305C>T
ENST00000682703.1:n.4131C>T
ENST00000682797.1:c.*255C>T	ENSP00000507582.1:n.*255C>T
ENST00000682985.1:c.674C>T	ENSP00000507598.1:p.Pro225Leu
ENST00000683433.1:c.422C>T	ENSP00000507463.1:p.Pro141Leu
ENST00000683685.1:n.2037C>T
ENST00000683710.1:c.*1130C>T	ENSP00000506785.1:n.*1130C>T
ENST00000683739.1:c.830C>T	ENSP00000507002.1:p.Pro277Leu
ENST00000683772.1:n.1207C>T
ENST00000684008.1:c.1101C>T	ENSP00000507962.1:n.1101C>T
ENST00000684190.1:c.1124C>T	ENSP00000507554.1:p.Pro375Leu
ENST00000684335.1:c.1052C>T	ENSP00000508112.1:p.Pro351Leu
XM_011522565.1:c.830C>T	XP_011520867.1:p.Pro277Leu
XM_017023457.2:c.1124C>T	XP_016878946.1:p.Pro375Leu
XM_017023458.1:c.830C>T	XP_016878947.1:p.Pro277Leu
XR_932882.3:n.1192C>T