Canonical Allele Identifier: CA3163721
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs763715960

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276192G>A , CM000666.2:g.186276192G>A GRCh38
NC_000004.11:g.187197346G>A , CM000666.1:g.187197346G>A GRCh37
NC_000004.10:g.187434340G>A NCBI36
NG_008051.1:g.15229G>A , LRG_583:g.15229G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.596-39G>A MANE Select ENSP00000384957.2:n.596-39G>A
ENST00000264692.8:c.434-39G>A ENSP00000264692.5:n.434-39G>A
ENST00000403665.6:c.596-39G>A ENSP00000384957.2:n.596-39G>A
ENST00000452239.1:c.43-39G>A
NM_000128.3:c.596-39G>A , LRG_583t1:c.596-39G>A NP_000119.1:n.596-39G>A
XM_005262821.2:c.596-39G>A XP_005262878.1:n.596-39G>A
XM_005262822.2:c.596-39G>A XP_005262879.1:n.596-39G>A
XM_005262823.2:c.485+1917G>A XP_005262880.1:n.485+1917G>A
XM_005262824.1:c.596-39G>A XP_005262881.1:n.596-39G>A
XM_006714137.1:c.596-39G>A XP_006714200.1:n.596-39G>A
XR_938706.1:n.948-39G>A
XR_938707.1:n.948-39G>A
XM_005262821.4:c.596-39G>A XP_005262878.1:n.596-39G>A
XM_005262822.4:c.596-39G>A XP_005262879.1:n.596-39G>A
XM_005262823.4:c.485+1917G>A XP_005262880.1:n.485+1917G>A
XM_006714137.3:c.596-39G>A XP_006714200.1:n.596-39G>A
XM_017007884.2:c.596-39G>A XP_016863373.1:n.596-39G>A
XM_017007885.2:c.596-39G>A XP_016863374.1:n.596-39G>A
XM_017007886.2:c.596-39G>A XP_016863375.1:n.596-39G>A
XR_001741172.2:n.929-39G>A
NM_000128.4:c.596-39G>A MANE Select NP_000119.1:n.596-39G>A