Canonical Allele Identifier: CA2671998007
Gene: AFG2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122938062_122938066del , CM000666.2:g.122938062_122938066del GRCh38
NC_000004.11:g.123859217_123859221del , CM000666.1:g.123859217_123859221del GRCh37
NC_000004.10:g.124078667_124078671del NCBI36
NG_051570.1:g.19993_19997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274008.5:c.1335-64_1335-60del MANE Select ENSP00000274008.3:n.1335-64_1335-60del
ENST00000674886.1:n.1397-64_1397-60del
ENST00000675612.1:c.1332-64_1332-60del ENSP00000502453.1:n.1332-64_1332-60del
ENST00000274008.4:c.1335-64_1335-60del ENSP00000274008.3:n.1335-64_1335-60del
ENST00000422835.2:n.1377-64_1377-60del
NM_145207.2:c.1335-64_1335-60del NP_660208.2:n.1335-64_1335-60del
XM_005262783.3:c.1332-64_1332-60del XP_005262840.1:n.1332-64_1332-60del
XM_011531678.1:c.1332-64_1332-60del XP_011529980.1:n.1332-64_1332-60del
XM_011531679.1:c.1335-64_1335-60del XP_011529981.1:n.1335-64_1335-60del
NM_001317799.1:c.1332-64_1332-60del NP_001304728.1:n.1332-64_1332-60del
NM_001345856.1:c.1332-64_1332-60del NP_001332785.1:n.1332-64_1332-60del
XM_011531678.2:c.1332-64_1332-60del XP_011529980.1:n.1332-64_1332-60del
XM_011531679.3:c.1335-64_1335-60del XP_011529981.1:n.1335-64_1335-60del
XM_017007825.1:c.1335-64_1335-60del XP_016863314.1:n.1335-64_1335-60del
XM_017007826.1:c.1335-64_1335-60del XP_016863315.1:n.1335-64_1335-60del
XM_017007827.2:c.1335-64_1335-60del XP_016863316.1:n.1335-64_1335-60del
XM_017007828.1:c.1113-64_1113-60del XP_016863317.1:n.1113-64_1113-60del
XM_017007829.1:c.879-64_879-60del XP_016863318.1:n.879-64_879-60del
XM_017007830.1:c.1335-64_1335-60del XP_016863319.1:n.1335-64_1335-60del
XR_001741151.1:n.1405-64_1405-60del
NM_145207.3:c.1335-64_1335-60del MANE Select NP_660208.2:n.1335-64_1335-60del
NM_001317799.2:c.1332-64_1332-60del NP_001304728.1:n.1332-64_1332-60del
NM_001345856.2:c.1332-64_1332-60del NP_001332785.1:n.1332-64_1332-60del