Canonical Allele Identifier: CA1071931761
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1739551248

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186266990_186266991dup , CM000666.2:g.186266990_186266991dup GRCh38
NC_000004.11:g.187188144_187188145dup , CM000666.1:g.187188144_187188145dup GRCh37
NC_000004.10:g.187425138_187425139dup NCBI36
NG_008051.1:g.6027_6028dup , LRG_583:g.6027_6028dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.-1-146_-1-145dup MANE Select ENSP00000384957.2:n.-1-146_-1-145dup
ENST00000264692.8:c.-1-146_-1-145dup ENSP00000264692.5:n.-1-146_-1-145dup
ENST00000403665.6:c.-1-146_-1-145dup ENSP00000384957.2:n.-1-146_-1-145dup
ENST00000492972.6:c.-1-146_-1-145dup ENSP00000424479.1:n.-1-146_-1-145dup
NM_000128.3:c.-1-146_-1-145dup , LRG_583t1:c.-1-146_-1-145dup NP_000119.1:n.-1-146_-1-145dup
XM_005262821.2:c.-1-146_-1-145dup XP_005262878.1:n.-1-146_-1-145dup
XM_005262822.2:c.-1-146_-1-145dup XP_005262879.1:n.-1-146_-1-145dup
XM_005262823.2:c.-1-146_-1-145dup XP_005262880.1:n.-1-146_-1-145dup
XM_005262824.1:c.-1-146_-1-145dup XP_005262881.1:n.-1-146_-1-145dup
XM_006714137.1:c.-1-146_-1-145dup XP_006714200.1:n.-1-146_-1-145dup
XR_938706.1:n.352-146_352-145dup
XR_938707.1:n.352-146_352-145dup
NM_001354804.1:c.-1-146_-1-145dup NP_001341733.1:n.-1-146_-1-145dup
XM_005262821.4:c.-1-146_-1-145dup XP_005262878.1:n.-1-146_-1-145dup
XM_005262822.4:c.-1-146_-1-145dup XP_005262879.1:n.-1-146_-1-145dup
XM_005262823.4:c.-1-146_-1-145dup XP_005262880.1:n.-1-146_-1-145dup
XM_006714137.3:c.-1-146_-1-145dup XP_006714200.1:n.-1-146_-1-145dup
XM_017007884.2:c.-1-146_-1-145dup XP_016863373.1:n.-1-146_-1-145dup
XM_017007885.2:c.-1-146_-1-145dup XP_016863374.1:n.-1-146_-1-145dup
XM_017007886.2:c.-1-146_-1-145dup XP_016863375.1:n.-1-146_-1-145dup
XR_001741172.2:n.333-146_333-145dup
NM_000128.4:c.-1-146_-1-145dup MANE Select NP_000119.1:n.-1-146_-1-145dup
NM_001354804.2:c.-1-146_-1-145dup NP_001341733.1:n.-1-146_-1-145dup