Canonical Allele Identifier: CA442642079
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187209945T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288791T>G , CM000666.2:g.186288791T>G GRCh38
NC_000004.11:g.187209945T>G , CM000666.1:g.187209945T>G GRCh37
NC_000004.10:g.187446939T>G NCBI36
NG_008051.1:g.27828T>G , LRG_583:g.27828T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*177T>G (F11) MANE Select ENSP00000384957.2:n.*177T>G
ENST00000264691.4:c.655T>G (F11)
NM_000128.3:c.*177T>G , LRG_583t1:c.*177T>G (F11) NP_000119.1:n.*177T>G
NR_033900.1:n.703A>C (F11-AS1)
XM_005262821.2:c.*177T>G (F11) XP_005262878.1:n.*177T>G
XM_005262822.2:c.*177T>G (F11) XP_005262879.1:n.*177T>G
XM_005262823.2:c.*177T>G (F11) XP_005262880.1:n.*177T>G
XM_006714137.1:c.*177T>G (F11) XP_006714200.1:n.*177T>G
XM_005262821.4:c.*177T>G (F11) XP_005262878.1:n.*177T>G
XM_005262822.4:c.*177T>G (F11) XP_005262879.1:n.*177T>G
XM_005262823.4:c.*177T>G (F11) XP_005262880.1:n.*177T>G
XM_006714137.3:c.*177T>G (F11) XP_006714200.1:n.*177T>G
NM_000128.4:c.*177T>G (F11) MANE Select NP_000119.1:n.*177T>G
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