Canonical Allele Identifier: CA1519926982
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186266073C= , CM000666.2:g.186266073C= GRCh38
NC_000004.11:g.187187227C= , CM000666.1:g.187187227C= GRCh37
NC_000004.10:g.187424221C= NCBI36
NG_008051.1:g.5110C= , LRG_583:g.5110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.6:c.-224C= ENSP00000384957.2:n.-224C=
NM_000128.3:c.-224C= , LRG_583t1:c.-224C= NP_000119.1:n.-224C=
XM_005262821.2:c.-224C= XP_005262878.1:n.-224C=
XM_005262822.2:c.-224C= XP_005262879.1:n.-224C=
XM_005262823.2:c.-224C= XP_005262880.1:n.-224C=
XM_005262824.1:c.-224C= XP_005262881.1:n.-224C=
XM_006714137.1:c.-224C= XP_006714200.1:n.-224C=
XR_938706.1:n.129C=
XR_938707.1:n.129C=
NM_001354804.1:c.-224C= NP_001341733.1:n.-224C=
XM_005262821.4:c.-224C= XP_005262878.1:n.-224C=
XM_005262822.4:c.-224C= XP_005262879.1:n.-224C=
XM_005262823.4:c.-224C= XP_005262880.1:n.-224C=
XM_006714137.3:c.-224C= XP_006714200.1:n.-224C=
XM_017007884.2:c.-224C= XP_016863373.1:n.-224C=
XM_017007885.2:c.-224C= XP_016863374.1:n.-224C=
XM_017007886.2:c.-224C= XP_016863375.1:n.-224C=
XR_001741172.2:n.110C=