Canonical Allele Identifier: CA2203685538
Gene: ALG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5080865_5080866delinsTA , CM000678.2:g.5080865_5080866delinsTA GRCh38
NC_000016.9:g.5130866_5130867delinsTA , CM000678.1:g.5130866_5130867delinsTA GRCh37
NC_000016.8:g.5070867_5070868delinsTA NCBI36
NG_009202.1:g.14057_14058delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000592793.6:n.3098-81_3098-80delinsTA
ENST00000682020.1:c.368-81_368-80delinsTA ENSP00000508075.1:n.368-81_368-80delinsTA
ENST00000682206.1:c.*54-81_*54-80delinsTA ENSP00000508285.1:n.*54-81_*54-80delinsTA
ENST00000682314.1:n.1010-81_1010-80delinsTA
ENST00000682327.1:c.434-81_434-80delinsTA ENSP00000507058.1:n.434-81_434-80delinsTA
ENST00000682349.1:n.3104-81_3104-80delinsTA
ENST00000682703.1:n.3930-81_3930-80delinsTA
ENST00000682797.1:c.*54-81_*54-80delinsTA ENSP00000507582.1:n.*54-81_*54-80delinsTA
ENST00000682985.1:c.473-81_473-80delinsTA ENSP00000507598.1:n.473-81_473-80delinsTA
ENST00000683433.1:c.218-81_218-80delinsTA ENSP00000507463.1:n.218-81_218-80delinsTA
ENST00000683685.1:n.1836-81_1836-80delinsTA
ENST00000683710.1:c.*929-81_*929-80delinsTA ENSP00000506785.1:n.*929-81_*929-80delinsTA
ENST00000683739.1:c.629-81_629-80delinsTA ENSP00000507002.1:n.629-81_629-80delinsTA
ENST00000683772.1:n.1006-81_1006-80delinsTA
ENST00000684008.1:c.900-81_900-80delinsTA ENSP00000507962.1:n.900-81_900-80delinsTA
ENST00000684190.1:c.923-81_923-80delinsTA ENSP00000507554.1:n.923-81_923-80delinsTA
ENST00000684335.1:c.961+1058_961+1059delinsTA ENSP00000508112.1:n.961+1058_961+1059delinsTA
ENST00000262374.10:c.962-81_962-80delinsTA MANE Select ENSP00000262374.5:n.962-81_962-80delinsTA
ENST00000650085.1:n.1786-81_1786-80delinsTA
ENST00000262374.9:c.962-81_962-80delinsTA ENSP00000262374.4:n.962-81_962-80delinsTA
ENST00000544428.1:c.629-81_629-80delinsTA ENSP00000440019.1:n.629-81_629-80delinsTA
ENST00000588623.5:c.629-81_629-80delinsTA ENSP00000468118.1:n.629-81_629-80delinsTA
ENST00000591822.5:c.*863-81_*863-80delinsTA ENSP00000467865.1:n.*863-81_*863-80delinsTA
NM_019109.4:c.962-81_962-80delinsTA NP_061982.3:n.962-81_962-80delinsTA
XM_011522565.1:c.629-81_629-80delinsTA XP_011520867.1:n.629-81_629-80delinsTA
XR_932882.1:n.1007-81_1007-80delinsTA
NM_001330504.1:c.629-81_629-80delinsTA NP_001317433.1:n.629-81_629-80delinsTA
XM_017023457.2:c.923-81_923-80delinsTA XP_016878946.1:n.923-81_923-80delinsTA
XM_017023458.1:c.629-81_629-80delinsTA XP_016878947.1:n.629-81_629-80delinsTA
XR_932882.3:n.991-81_991-80delinsTA
NM_019109.5:c.962-81_962-80delinsTA MANE Select NP_061982.3:n.962-81_962-80delinsTA
NM_001330504.2:c.629-81_629-80delinsTA NP_001317433.1:n.629-81_629-80delinsTA