Canonical Allele Identifier: CA565880221

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs1443153067
• gnomAD v2: 6-29697069-GCCT-G
• gnomAD v3: 6-29729292-GCCT-G
• gnomAD v4: 6-29729292-GCCT-G
• MyVariant Identifiers: chr6:g.29697070_29697072del (hg19) ; chr6:g.29729293_29729295del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729298_29729300del , CM000668.2:g.29729298_29729300del	GRCh38
NC_000006.11:g.29697075_29697077del , CM000668.1:g.29697075_29697077del	GRCh37
NC_000006.10:g.29805054_29805056del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465459.2:c.403+3255_403+3257del (HLA-F)	ENSP00000486947.1:n.403+3255_403+3257del
ENST00000475996.1:c.1452_1454del (HLA-F)
NR_026972.1:n.1236-800_1236-798del (HLA-F-AS1)
NR_026973.1:n.151-2156_151-2154del (HLA-F-AS1)
XM_011514563.1:c.1003+3735_1003+3737del (HLA-F)	XP_011512865.1:n.1003+3735_1003+3737del
XM_011514564.1:c.1003+3735_1003+3737del (HLA-F)	XP_011512866.1:n.1003+3735_1003+3737del
XM_017010810.1:c.*1192_*1194del (HLA-F)	XP_016866299.1:n.*1192_*1194del
XM_017010813.1:c.1158+2294_1158+2296del (HLA-F)	XP_016866302.1:n.1158+2294_1158+2296del
XR_001743373.1:n.1188+2294_1188+2296del (HLA-F)
XR_001743374.1:n.1188+2294_1188+2296del (HLA-F)
XR_001743376.1:n.1131+2294_1131+2296del (HLA-F)