Canonical Allele Identifier: CA442640467
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187207288A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186286134A>G , CM000666.2:g.186286134A>G GRCh38
NC_000004.11:g.187207288A>G , CM000666.1:g.187207288A>G GRCh37
NC_000004.10:g.187444282A>G NCBI36
NG_008051.1:g.25171A>G , LRG_583:g.25171A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1481-281A>G (F11) MANE Select ENSP00000384957.2:n.1481-281A>G
ENST00000264691.4:c.176+321A>G (F11)
ENST00000264692.8:c.1319-281A>G (F11) ENSP00000264692.5:n.1319-281A>G
ENST00000403665.6:c.1481-281A>G (F11) ENSP00000384957.2:n.1481-281A>G
NM_000128.3:c.1481-281A>G , LRG_583t1:c.1481-281A>G (F11) NP_000119.1:n.1481-281A>G
NR_033900.1:n.1199T>C (F11-AS1)
XM_005262821.2:c.1484-281A>G (F11) XP_005262878.1:n.1484-281A>G
XM_005262822.2:c.1483+321A>G (F11) XP_005262879.1:n.1483+321A>G
XM_005262823.2:c.1214-281A>G (F11) XP_005262880.1:n.1214-281A>G
XM_005262824.1:c.1483+321A>G (F11) XP_005262881.1:n.1483+321A>G
XM_006714137.1:c.1436-281A>G (F11) XP_006714200.1:n.1436-281A>G
XR_938706.1:n.1889-281A>G (F11)
XR_938707.1:n.1888+321A>G (F11)
XM_005262821.4:c.1484-281A>G (F11) XP_005262878.1:n.1484-281A>G
XM_005262822.4:c.1483+321A>G (F11) XP_005262879.1:n.1483+321A>G
XM_005262823.4:c.1214-281A>G (F11) XP_005262880.1:n.1214-281A>G
XM_006714137.3:c.1436-281A>G (F11) XP_006714200.1:n.1436-281A>G
XR_001741172.2:n.1955-281A>G (F11)
NM_000128.4:c.1481-281A>G (F11) MANE Select NP_000119.1:n.1481-281A>G
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