Canonical Allele Identifier: CA1335660672
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233264789_233264792delinsATGT , CM000664.2:g.233264789_233264792delinsATGT GRCh38
NC_000002.11:g.234173435_234173438delinsATGT , CM000664.1:g.234173435_234173438delinsATGT GRCh37
NC_000002.10:g.233838174_233838177delinsATGT NCBI36
NG_023038.1:g.18219_18222delinsATGT

Transcript Alleles

HGVS Amino-acid change
ENST00000392017.9:c.390-103_390-100delinsATGT MANE Select ENSP00000375872.4:n.390-103_390-100delins...
ENST00000347464.9:c.210-5213_210-5210delinsATGT ENSP00000318259.6:n.210-5213_210-5210deli...
ENST00000373525.9:c.210-5213_210-5210delinsATGT ENSP00000362625.5:n.210-5213_210-5210deli...
ENST00000392017.8:c.390-103_390-100delinsATGT ENSP00000375872.4:n.390-103_390-100delins...
ENST00000392018.1:c.390-103_390-100delinsATGT ENSP00000375873.1:n.390-103_390-100delins...
ENST00000392020.8:c.390-103_390-100delinsATGT ENSP00000375875.4:n.390-103_390-100delins...
ENST00000392021.7:c.*271-103_*271-100delinsATGT ENSP00000375876.3:n.*271-103_*271-100deli...
ENST00000417017.5:c.389+724_389+727delinsATGT ENSP00000412046.1:n.389+724_389+727delins...
ENST00000419681.5:c.210-5213_210-5210delinsATGT ENSP00000398773.1:n.210-5213_210-5210deli...
ENST00000431917.5:c.138-103_138-100delinsATGT ENSP00000397512.1:n.138-103_138-100delins...
ENST00000444735.5:c.210-5213_210-5210delinsATGT ENSP00000409215.1:n.210-5213_210-5210deli...
ENST00000474148.5:n.517-103_517-100delinsATGT
ENST00000479942.5:n.536-103_536-100delinsATGT
NM_001190266.1:c.138-103_138-100delinsATGT NP_001177195.1:n.138-103_138-100delinsATG...
NM_001190267.1:c.42-103_42-100delinsATGT NP_001177196.1:n.42-103_42-100delinsATGT
NM_017974.3:c.390-103_390-100delinsATGT NP_060444.3:n.390-103_390-100delinsATGT
NM_030803.6:c.390-103_390-100delinsATGT NP_110430.5:n.390-103_390-100delinsATGT
NM_198890.2:c.210-5213_210-5210delinsATGT NP_942593.2:n.210-5213_210-5210delinsATGT...
XM_005246082.1:c.390-103_390-100delinsATGT XP_005246139.1:n.390-103_390-100delinsATG...
XM_005246084.1:c.210-5213_210-5210delinsATGT XP_005246141.1:n.210-5213_210-5210delinsA...
XM_005246086.1:c.210-5213_210-5210delinsATGT XP_005246143.1:n.210-5213_210-5210delinsA...
XM_006712608.1:c.389+724_389+727delinsATGT XP_006712671.1:n.389+724_389+727delinsATG...
XR_241242.1:n.584-103_584-100delinsATGT
NM_001363742.1:c.390-103_390-100delinsATGT NP_001350671.1:n.390-103_390-100delinsATG...
XM_005246084.2:c.210-5213_210-5210delinsATGT XP_005246141.1:n.210-5213_210-5210delinsA...
XM_005246086.2:c.210-5213_210-5210delinsATGT XP_005246143.1:n.210-5213_210-5210delinsA...
XM_006712608.3:c.389+724_389+727delinsATGT XP_006712671.1:n.389+724_389+727delinsATG...
XR_001738801.2:n.571-103_571-100delinsATGT
XR_241242.3:n.571-103_571-100delinsATGT
NM_030803.7:c.390-103_390-100delinsATGT MANE Select NP_110430.5:n.390-103_390-100delinsATGT
NM_001190266.2:c.138-103_138-100delinsATGT NP_001177195.1:n.138-103_138-100delinsATG...
NM_001190267.2:c.42-103_42-100delinsATGT NP_001177196.1:n.42-103_42-100delinsATGT
NM_001363742.2:c.390-103_390-100delinsATGT NP_001350671.1:n.390-103_390-100delinsATG...
NM_017974.4:c.390-103_390-100delinsATGT NP_060444.3:n.390-103_390-100delinsATGT
NM_198890.3:c.210-5213_210-5210delinsATGT NP_942593.2:n.210-5213_210-5210delinsATGT...