Canonical Allele Identifier: CA2671998014
Gene: AFG2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122938070_122938079del , CM000666.2:g.122938070_122938079del GRCh38
NC_000004.11:g.123859225_123859234del , CM000666.1:g.123859225_123859234del GRCh37
NC_000004.10:g.124078675_124078684del NCBI36
NG_051570.1:g.20001_20010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274008.5:c.1335-56_1335-47del MANE Select ENSP00000274008.3:n.1335-56_1335-47del
ENST00000674886.1:n.1397-56_1397-47del
ENST00000675612.1:c.1332-56_1332-47del ENSP00000502453.1:n.1332-56_1332-47del
ENST00000274008.4:c.1335-56_1335-47del ENSP00000274008.3:n.1335-56_1335-47del
ENST00000422835.2:n.1377-56_1377-47del
NM_145207.2:c.1335-56_1335-47del NP_660208.2:n.1335-56_1335-47del
XM_005262783.3:c.1332-56_1332-47del XP_005262840.1:n.1332-56_1332-47del
XM_011531678.1:c.1332-56_1332-47del XP_011529980.1:n.1332-56_1332-47del
XM_011531679.1:c.1335-56_1335-47del XP_011529981.1:n.1335-56_1335-47del
NM_001317799.1:c.1332-56_1332-47del NP_001304728.1:n.1332-56_1332-47del
NM_001345856.1:c.1332-56_1332-47del NP_001332785.1:n.1332-56_1332-47del
XM_011531678.2:c.1332-56_1332-47del XP_011529980.1:n.1332-56_1332-47del
XM_011531679.3:c.1335-56_1335-47del XP_011529981.1:n.1335-56_1335-47del
XM_017007825.1:c.1335-56_1335-47del XP_016863314.1:n.1335-56_1335-47del
XM_017007826.1:c.1335-56_1335-47del XP_016863315.1:n.1335-56_1335-47del
XM_017007827.2:c.1335-56_1335-47del XP_016863316.1:n.1335-56_1335-47del
XM_017007828.1:c.1113-56_1113-47del XP_016863317.1:n.1113-56_1113-47del
XM_017007829.1:c.879-56_879-47del XP_016863318.1:n.879-56_879-47del
XM_017007830.1:c.1335-56_1335-47del XP_016863319.1:n.1335-56_1335-47del
XR_001741151.1:n.1405-56_1405-47del
NM_145207.3:c.1335-56_1335-47del MANE Select NP_660208.2:n.1335-56_1335-47del
NM_001317799.2:c.1332-56_1332-47del NP_001304728.1:n.1332-56_1332-47del
NM_001345856.2:c.1332-56_1332-47del NP_001332785.1:n.1332-56_1332-47del