Canonical Allele Identifier: CA358945593
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187208905A>C (hg19) chr4:g.186287751A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287751A>C , CM000666.2:g.186287751A>C GRCh38
NC_000004.11:g.187208905A>C , CM000666.1:g.187208905A>C GRCh37
NC_000004.10:g.187445899A>C NCBI36
NG_008051.1:g.26788A>C , LRG_583:g.26788A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1644A>C (F11) MANE Select ENSP00000384957.2:p.Arg548Ser
ENST00000264691.4:c.244A>C (F11)
ENST00000264692.8:c.1482A>C (F11) ENSP00000264692.5:p.Arg494Ser
ENST00000403665.6:c.1644A>C (F11) ENSP00000384957.2:p.Arg548Ser
ENST00000503841.1:n.163A>C (F11)
NM_000128.3:c.1644A>C , LRG_583t1:c.1644A>C (F11) NP_000119.1:p.Arg548Ser
NR_033900.1:n.1066+677T>G (F11-AS1)
XM_005262821.2:c.1647A>C (F11) XP_005262878.1:p.Arg549Ser
XM_005262822.2:c.1551A>C (F11) XP_005262879.1:p.Arg517Ser
XM_005262823.2:c.1377A>C (F11) XP_005262880.1:p.Arg459Ser
XM_006714137.1:c.1599A>C (F11) XP_006714200.1:p.Arg533Ser
XR_938707.1:n.1956A>C (F11)
XM_005262821.4:c.1647A>C (F11) XP_005262878.1:p.Arg549Ser
XM_005262822.4:c.1551A>C (F11) XP_005262879.1:p.Arg517Ser
XM_005262823.4:c.1377A>C (F11) XP_005262880.1:p.Arg459Ser
XM_006714137.3:c.1599A>C (F11) XP_006714200.1:p.Arg533Ser
NM_000128.4:c.1644A>C (F11) MANE Select NP_000119.1:p.Arg548Ser
Search 100 bp 5'
Search 100 bp 3'