Canonical Allele Identifier: CA1335660668
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233264760_233264762delinsTAA , CM000664.2:g.233264760_233264762delinsTAA GRCh38
NC_000002.11:g.234173406_234173408delinsTAA , CM000664.1:g.234173406_234173408delinsTAA GRCh37
NC_000002.10:g.233838145_233838147delinsTAA NCBI36
NG_023038.1:g.18190_18192delinsTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000392017.9:c.390-132_390-130delinsTAA MANE Select ENSP00000375872.4:n.390-132_390-130delins...
ENST00000347464.9:c.210-5242_210-5240delinsTAA ENSP00000318259.6:n.210-5242_210-5240deli...
ENST00000373525.9:c.210-5242_210-5240delinsTAA ENSP00000362625.5:n.210-5242_210-5240deli...
ENST00000392017.8:c.390-132_390-130delinsTAA ENSP00000375872.4:n.390-132_390-130delins...
ENST00000392018.1:c.390-132_390-130delinsTAA ENSP00000375873.1:n.390-132_390-130delins...
ENST00000392020.8:c.390-132_390-130delinsTAA ENSP00000375875.4:n.390-132_390-130delins...
ENST00000392021.7:c.*271-132_*271-130delinsTAA ENSP00000375876.3:n.*271-132_*271-130deli...
ENST00000417017.5:c.389+695_389+697delinsTAA ENSP00000412046.1:n.389+695_389+697delins...
ENST00000419681.5:c.210-5242_210-5240delinsTAA ENSP00000398773.1:n.210-5242_210-5240deli...
ENST00000431917.5:c.138-132_138-130delinsTAA ENSP00000397512.1:n.138-132_138-130delins...
ENST00000444735.5:c.210-5242_210-5240delinsTAA ENSP00000409215.1:n.210-5242_210-5240deli...
ENST00000474148.5:n.517-132_517-130delinsTAA
ENST00000479942.5:n.536-132_536-130delinsTAA
NM_001190266.1:c.138-132_138-130delinsTAA NP_001177195.1:n.138-132_138-130delinsTAA...
NM_001190267.1:c.42-132_42-130delinsTAA NP_001177196.1:n.42-132_42-130delinsTAA
NM_017974.3:c.390-132_390-130delinsTAA NP_060444.3:n.390-132_390-130delinsTAA
NM_030803.6:c.390-132_390-130delinsTAA NP_110430.5:n.390-132_390-130delinsTAA
NM_198890.2:c.210-5242_210-5240delinsTAA NP_942593.2:n.210-5242_210-5240delinsTAA
XM_005246082.1:c.390-132_390-130delinsTAA XP_005246139.1:n.390-132_390-130delinsTAA...
XM_005246084.1:c.210-5242_210-5240delinsTAA XP_005246141.1:n.210-5242_210-5240delinsT...
XM_005246086.1:c.210-5242_210-5240delinsTAA XP_005246143.1:n.210-5242_210-5240delinsT...
XM_006712608.1:c.389+695_389+697delinsTAA XP_006712671.1:n.389+695_389+697delinsTAA...
XR_241242.1:n.584-132_584-130delinsTAA
NM_001363742.1:c.390-132_390-130delinsTAA NP_001350671.1:n.390-132_390-130delinsTAA...
XM_005246084.2:c.210-5242_210-5240delinsTAA XP_005246141.1:n.210-5242_210-5240delinsT...
XM_005246086.2:c.210-5242_210-5240delinsTAA XP_005246143.1:n.210-5242_210-5240delinsT...
XM_006712608.3:c.389+695_389+697delinsTAA XP_006712671.1:n.389+695_389+697delinsTAA...
XR_001738801.2:n.571-132_571-130delinsTAA
XR_241242.3:n.571-132_571-130delinsTAA
NM_030803.7:c.390-132_390-130delinsTAA MANE Select NP_110430.5:n.390-132_390-130delinsTAA
NM_001190266.2:c.138-132_138-130delinsTAA NP_001177195.1:n.138-132_138-130delinsTAA...
NM_001190267.2:c.42-132_42-130delinsTAA NP_001177196.1:n.42-132_42-130delinsTAA
NM_001363742.2:c.390-132_390-130delinsTAA NP_001350671.1:n.390-132_390-130delinsTAA...
NM_017974.4:c.390-132_390-130delinsTAA NP_060444.3:n.390-132_390-130delinsTAA
NM_198890.3:c.210-5242_210-5240delinsTAA NP_942593.2:n.210-5242_210-5240delinsTAA