Canonical Allele Identifier: CA792348313
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1405270640

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186265960dup , CM000666.2:g.186265960dup GRCh38
NC_000004.11:g.187187114dup , CM000666.1:g.187187114dup GRCh37
NC_000004.10:g.187424108dup NCBI36
NG_008051.1:g.4997dup , LRG_583:g.4997dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-337dup ENSP00000384957.2:n.-337dup
XM_005262821.2:c.-337dup XP_005262878.1:n.-337dup
XM_005262822.2:c.-337dup XP_005262879.1:n.-337dup
XM_005262823.2:c.-337dup XP_005262880.1:n.-337dup
XM_005262824.1:c.-337dup XP_005262881.1:n.-337dup
XM_006714137.1:c.-337dup XP_006714200.1:n.-337dup
XR_938706.1:n.16dup
XR_938707.1:n.16dup