Canonical Allele Identifier: CA786421281
Gene: AFG2A HGNC NCBI

Linked Data

dbSNP Id: rs1320836685

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122938074_122938075del , CM000666.2:g.122938074_122938075del GRCh38
NC_000004.11:g.123859229_123859230del , CM000666.1:g.123859229_123859230del GRCh37
NC_000004.10:g.124078679_124078680del NCBI36
NG_051570.1:g.20005_20006del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274008.5:c.1335-52_1335-51del MANE Select ENSP00000274008.3:n.1335-52_1335-51del
ENST00000674886.1:n.1397-52_1397-51del
ENST00000675612.1:c.1332-52_1332-51del ENSP00000502453.1:n.1332-52_1332-51del
ENST00000274008.4:c.1335-52_1335-51del ENSP00000274008.3:n.1335-52_1335-51del
ENST00000422835.2:n.1377-52_1377-51del
NM_145207.2:c.1335-52_1335-51del NP_660208.2:n.1335-52_1335-51del
XM_005262783.3:c.1332-52_1332-51del XP_005262840.1:n.1332-52_1332-51del
XM_011531678.1:c.1332-52_1332-51del XP_011529980.1:n.1332-52_1332-51del
XM_011531679.1:c.1335-52_1335-51del XP_011529981.1:n.1335-52_1335-51del
NM_001317799.1:c.1332-52_1332-51del NP_001304728.1:n.1332-52_1332-51del
NM_001345856.1:c.1332-52_1332-51del NP_001332785.1:n.1332-52_1332-51del
XM_011531678.2:c.1332-52_1332-51del XP_011529980.1:n.1332-52_1332-51del
XM_011531679.3:c.1335-52_1335-51del XP_011529981.1:n.1335-52_1335-51del
XM_017007825.1:c.1335-52_1335-51del XP_016863314.1:n.1335-52_1335-51del
XM_017007826.1:c.1335-52_1335-51del XP_016863315.1:n.1335-52_1335-51del
XM_017007827.2:c.1335-52_1335-51del XP_016863316.1:n.1335-52_1335-51del
XM_017007828.1:c.1113-52_1113-51del XP_016863317.1:n.1113-52_1113-51del
XM_017007829.1:c.879-52_879-51del XP_016863318.1:n.879-52_879-51del
XM_017007830.1:c.1335-52_1335-51del XP_016863319.1:n.1335-52_1335-51del
XR_001741151.1:n.1405-52_1405-51del
NM_145207.3:c.1335-52_1335-51del MANE Select NP_660208.2:n.1335-52_1335-51del
NM_001317799.2:c.1332-52_1332-51del NP_001304728.1:n.1332-52_1332-51del
NM_001345856.2:c.1332-52_1332-51del NP_001332785.1:n.1332-52_1332-51del