Canonical Allele Identifier: CA1519935956
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280211T= , CM000666.2:g.186280211T= GRCh38
NC_000004.11:g.187201365T= , CM000666.1:g.187201365T= GRCh37
NC_000004.10:g.187438359T= NCBI36
NG_008051.1:g.19248T= , LRG_583:g.19248T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.866-12T= MANE Select ENSP00000384957.2:n.866-12T=
ENST00000264692.8:c.704-12T= ENSP00000264692.5:n.704-12T=
ENST00000403665.6:c.866-12T= ENSP00000384957.2:n.866-12T=
ENST00000452239.1:c.313-12T=
NM_000128.3:c.866-12T= , LRG_583t1:c.866-12T= NP_000119.1:n.866-12T=
XM_005262821.2:c.866-12T= XP_005262878.1:n.866-12T=
XM_005262822.2:c.866-12T= XP_005262879.1:n.866-12T=
XM_005262823.2:c.596-12T= XP_005262880.1:n.596-12T=
XM_005262824.1:c.866-12T= XP_005262881.1:n.866-12T=
XM_006714137.1:c.866-60T= XP_006714200.1:n.866-60T=
XR_938706.1:n.1218-12T=
XR_938707.1:n.1218-12T=
XM_005262821.4:c.866-12T= XP_005262878.1:n.866-12T=
XM_005262822.4:c.866-12T= XP_005262879.1:n.866-12T=
XM_005262823.4:c.596-12T= XP_005262880.1:n.596-12T=
XM_006714137.3:c.866-60T= XP_006714200.1:n.866-60T=
XM_017007884.2:c.866-12T= XP_016863373.1:n.866-12T=
XM_017007885.2:c.866-12T= XP_016863374.1:n.866-12T=
XM_017007886.2:c.866-12T= XP_016863375.1:n.866-12T=
XR_001741172.2:n.1199-12T=
NM_000128.4:c.866-12T= MANE Select NP_000119.1:n.866-12T=