Canonical Allele Identifier: CA2672904208
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186288845-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288847del , CM000666.2:g.186288847del GRCh38
NC_000004.11:g.187210001del , CM000666.1:g.187210001del GRCh37
NC_000004.10:g.187446995del NCBI36
NG_008051.1:g.27884del , LRG_583:g.27884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*233del (F11) MANE Select ENSP00000384957.2:n.*233del
NM_000128.3:c.*233del , LRG_583t1:c.*233del (F11) NP_000119.1:n.*233del
NR_033900.1:n.648del (F11-AS1)
XM_005262821.2:c.*233del (F11) XP_005262878.1:n.*233del
XM_005262822.2:c.*233del (F11) XP_005262879.1:n.*233del
XM_005262823.2:c.*233del (F11) XP_005262880.1:n.*233del
XM_006714137.1:c.*233del (F11) XP_006714200.1:n.*233del
XM_005262821.4:c.*233del (F11) XP_005262878.1:n.*233del
XM_005262822.4:c.*233del (F11) XP_005262879.1:n.*233del
XM_005262823.4:c.*233del (F11) XP_005262880.1:n.*233del
XM_006714137.3:c.*233del (F11) XP_006714200.1:n.*233del
NM_000128.4:c.*233del (F11) MANE Select NP_000119.1:n.*233del
Search 100 bp 5'
Search 100 bp 3'