Canonical Allele Identifier: CA358938679
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1740719412

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280497C>T , CM000666.2:g.186280497C>T GRCh38
NC_000004.11:g.187201651C>T , CM000666.1:g.187201651C>T GRCh37
NC_000004.10:g.187438645C>T NCBI36
NG_008051.1:g.19534C>T , LRG_583:g.19534C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1052C>T MANE Select ENSP00000384957.2:p.Ser351Phe
ENST00000264692.8:c.890C>T ENSP00000264692.5:p.Ser297Phe
ENST00000403665.6:c.1052C>T ENSP00000384957.2:p.Ser351Phe
ENST00000452239.1:c.499C>T
NM_000128.3:c.1052C>T , LRG_583t1:c.1052C>T NP_000119.1:p.Ser351Phe
XM_005262821.2:c.1055C>T XP_005262878.1:p.Ser352Phe
XM_005262822.2:c.1055C>T XP_005262879.1:p.Ser352Phe
XM_005262823.2:c.785C>T XP_005262880.1:p.Ser262Phe
XM_005262824.1:c.1055C>T XP_005262881.1:p.Ser352Phe
XM_006714137.1:c.1007C>T XP_006714200.1:p.Ser336Phe
XR_938706.1:n.1407C>T
XR_938707.1:n.1407C>T
XM_005262821.4:c.1055C>T XP_005262878.1:p.Ser352Phe
XM_005262822.4:c.1055C>T XP_005262879.1:p.Ser352Phe
XM_005262823.4:c.785C>T XP_005262880.1:p.Ser262Phe
XM_006714137.3:c.1007C>T XP_006714200.1:p.Ser336Phe
XM_017007884.2:c.1055C>T XP_016863373.1:p.Ser352Phe
XM_017007885.2:c.1055C>T XP_016863374.1:p.Ser352Phe
XM_017007886.2:c.1052C>T XP_016863375.1:p.Ser351Phe
XR_001741172.2:n.1473C>T
NM_000128.4:c.1052C>T MANE Select NP_000119.1:p.Ser351Phe