Canonical Allele Identifier: CA358958390
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186274118T>G , CM000666.2:g.186274118T>G GRCh38
NC_000004.11:g.187195272T>G , CM000666.1:g.187195272T>G GRCh37
NC_000004.10:g.187432266T>G NCBI36
NG_008051.1:g.13155T>G , LRG_583:g.13155T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.328T>G MANE Select ENSP00000384957.2:p.Cys110Gly
ENST00000264692.8:c.323+943T>G ENSP00000264692.5:n.323+943T>G
ENST00000403665.6:c.328T>G ENSP00000384957.2:p.Cys110Gly
ENST00000492972.6:c.328T>G ENSP00000424479.1:p.Cys110Gly
ENST00000514715.1:n.200T>G
NM_000128.3:c.328T>G , LRG_583t1:c.328T>G NP_000119.1:p.Cys110Gly
XM_005262821.2:c.328T>G XP_005262878.1:p.Cys110Gly
XM_005262822.2:c.328T>G XP_005262879.1:p.Cys110Gly
XM_005262823.2:c.328T>G XP_005262880.1:p.Cys110Gly
XM_005262824.1:c.328T>G XP_005262881.1:p.Cys110Gly
XM_006714137.1:c.328T>G XP_006714200.1:p.Cys110Gly
XR_938706.1:n.680T>G
XR_938707.1:n.680T>G
NM_001354804.1:c.328T>G NP_001341733.1:p.Cys110Gly
XM_005262821.4:c.328T>G XP_005262878.1:p.Cys110Gly
XM_005262822.4:c.328T>G XP_005262879.1:p.Cys110Gly
XM_005262823.4:c.328T>G XP_005262880.1:p.Cys110Gly
XM_006714137.3:c.328T>G XP_006714200.1:p.Cys110Gly
XM_017007884.2:c.328T>G XP_016863373.1:p.Cys110Gly
XM_017007885.2:c.328T>G XP_016863374.1:p.Cys110Gly
XM_017007886.2:c.328T>G XP_016863375.1:p.Cys110Gly
XR_001741172.2:n.661T>G
NM_000128.4:c.328T>G MANE Select NP_000119.1:p.Cys110Gly
NM_001354804.2:c.328T>G NP_001341733.1:p.Cys110Gly