Canonical Allele Identifier: CA916800807

Gene: ATG16L1 SCARNA5

Linked Data

• dbSNP Id: rs1574875443

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233275819_233275820insAG , CM000664.2:g.233275819_233275820insAG	GRCh38
NC_000002.11:g.234184465_234184466insAG , CM000664.1:g.234184465_234184466insAG	GRCh37
NC_000002.10:g.233849204_233849205insAG	NCBI36
NG_023038.1:g.29249_29250insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.954+1041_954+1042insAG (ATG16L1) MANE Select	ENSP00000375872.4:n.954+1041_954+1042insAG
ENST00000347464.9:c.465+1041_465+1042insAG (ATG16L1)	ENSP00000318259.6:n.465+1041_465+1042insAG
ENST00000373525.9:c.522+1041_522+1042insAG (ATG16L1)	ENSP00000362625.5:n.522+1041_522+1042insAG
ENST00000392017.8:c.954+1041_954+1042insAG (ATG16L1)	ENSP00000375872.4:n.954+1041_954+1042insAG
ENST00000392018.1:c.1005+1041_1005+1042insAG (ATG16L1)	ENSP00000375873.1:n.1005+1041_1005+1042insAG
ENST00000392020.8:c.897+1041_897+1042insAG (ATG16L1)	ENSP00000375875.4:n.897+1041_897+1042insAG
ENST00000392021.7:c.*835+1041_*835+1042insAG (ATG16L1)	ENSP00000375876.3:n.*835+1041_*835+1042insAG
ENST00000419681.5:c.465+1041_465+1042insAG (ATG16L1)	ENSP00000398773.1:n.465+1041_465+1042insAG
ENST00000464645.5:n.89+352_89+353insAG (ATG16L1)
ENST00000474148.5:n.1749+1041_1749+1042insAG (ATG16L1)
ENST00000479942.5:n.1100+1041_1100+1042insAG (ATG16L1)
ENST00000492298.5:n.475+1041_475+1042insAG (ATG16L1)
ENST00000498620.5:n.461+1041_461+1042insAG (ATG16L1)
NM_001190266.1:c.702+1041_702+1042insAG (ATG16L1)	NP_001177195.1:n.702+1041_702+1042insAG
NM_001190267.1:c.606+1041_606+1042insAG (ATG16L1)	NP_001177196.1:n.606+1041_606+1042insAG
NM_017974.3:c.897+1041_897+1042insAG (ATG16L1)	NP_060444.3:n.897+1041_897+1042insAG
NM_030803.6:c.954+1041_954+1042insAG (ATG16L1)	NP_110430.5:n.954+1041_954+1042insAG
NM_198890.2:c.465+1041_465+1042insAG (ATG16L1)	NP_942593.2:n.465+1041_465+1042insAG
NR_003008.2:n.94_95insAG (SCARNA5)
XM_005246082.1:c.1005+1041_1005+1042insAG (ATG16L1)	XP_005246139.1:n.1005+1041_1005+1042insAG
XM_005246084.1:c.573+1041_573+1042insAG (ATG16L1)	XP_005246141.1:n.573+1041_573+1042insAG
XM_005246086.1:c.522+1041_522+1042insAG (ATG16L1)	XP_005246143.1:n.522+1041_522+1042insAG
XM_006712608.1:c.753+1041_753+1042insAG (ATG16L1)	XP_006712671.1:n.753+1041_753+1042insAG
XR_241242.1:n.1199+1041_1199+1042insAG (ATG16L1)
NM_001363742.1:c.1005+1041_1005+1042insAG (ATG16L1)	NP_001350671.1:n.1005+1041_1005+1042insAG
XM_005246084.2:c.573+1041_573+1042insAG (ATG16L1)	XP_005246141.1:n.573+1041_573+1042insAG
XM_005246086.2:c.522+1041_522+1042insAG (ATG16L1)	XP_005246143.1:n.522+1041_522+1042insAG
XM_006712608.3:c.753+1041_753+1042insAG (ATG16L1)	XP_006712671.1:n.753+1041_753+1042insAG
XR_001738801.2:n.1135+1041_1135+1042insAG (ATG16L1)
XR_241242.3:n.1186+1041_1186+1042insAG (ATG16L1)
NM_030803.7:c.954+1041_954+1042insAG (ATG16L1) MANE Select	NP_110430.5:n.954+1041_954+1042insAG
NM_001190266.2:c.702+1041_702+1042insAG (ATG16L1)	NP_001177195.1:n.702+1041_702+1042insAG
NM_001190267.2:c.606+1041_606+1042insAG (ATG16L1)	NP_001177196.1:n.606+1041_606+1042insAG
NM_001363742.2:c.1005+1041_1005+1042insAG (ATG16L1)	NP_001350671.1:n.1005+1041_1005+1042insAG
NM_017974.4:c.897+1041_897+1042insAG (ATG16L1)	NP_060444.3:n.897+1041_897+1042insAG
NM_198890.3:c.465+1041_465+1042insAG (ATG16L1)	NP_942593.2:n.465+1041_465+1042insAG