Canonical Allele Identifier: CA1618422309
Gene: HLA-F HGNC NCBI
HLA-F-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29729171_29729175delinsAGCCT , CM000668.2:g.29729171_29729175delinsAGCCT GRCh38
NC_000006.11:g.29696948_29696952delinsAGCCT , CM000668.1:g.29696948_29696952delinsAGCCT GRCh37
NC_000006.10:g.29804927_29804931delinsAGCCT NCBI36
NG_012009.1:g.10832_10836delinsAGCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465459.2:c.403+3128_403+3132delinsAGCCT (HLA-F) ENSP00000486947.1:n.403+3128_403+3132delinsAGCCT
ENST00000475996.1:c.1325_1329delinsAGCCT (HLA-F)
NR_026972.1:n.1236-680_1236-676delinsAGGCT (HLA-F-AS1)
NR_026973.1:n.151-2036_151-2032delinsAGGCT (HLA-F-AS1)
XM_011514563.1:c.1003+3608_1003+3612delinsAGCCT (HLA-F) XP_011512865.1:n.1003+3608_1003+3612delinsAGCCT
XM_011514564.1:c.1003+3608_1003+3612delinsAGCCT (HLA-F) XP_011512866.1:n.1003+3608_1003+3612delinsAGCCT
XM_017010810.1:c.*1065_*1069delinsAGCCT (HLA-F) XP_016866299.1:n.*1065_*1069delinsAGCCT
XM_017010813.1:c.1158+2167_1158+2171delinsAGCCT (HLA-F) XP_016866302.1:n.1158+2167_1158+2171delinsAGCCT
XR_001743373.1:n.1188+2167_1188+2171delinsAGCCT (HLA-F)
XR_001743374.1:n.1188+2167_1188+2171delinsAGCCT (HLA-F)
XR_001743376.1:n.1131+2167_1131+2171delinsAGCCT (HLA-F)