Canonical Allele Identifier: CA358937553
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs758385654

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280234T>C , CM000666.2:g.186280234T>C GRCh38
NC_000004.11:g.187201388T>C , CM000666.1:g.187201388T>C GRCh37
NC_000004.10:g.187438382T>C NCBI36
NG_008051.1:g.19271T>C , LRG_583:g.19271T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.877T>C MANE Select ENSP00000384957.2:p.Ser293Pro
ENST00000264692.8:c.715T>C ENSP00000264692.5:p.Ser239Pro
ENST00000403665.6:c.877T>C ENSP00000384957.2:p.Ser293Pro
ENST00000452239.1:c.324T>C
NM_000128.3:c.877T>C , LRG_583t1:c.877T>C NP_000119.1:p.Ser293Pro
XM_005262821.2:c.877T>C XP_005262878.1:p.Ser293Pro
XM_005262822.2:c.877T>C XP_005262879.1:p.Ser293Pro
XM_005262823.2:c.607T>C XP_005262880.1:p.Ser203Pro
XM_005262824.1:c.877T>C XP_005262881.1:p.Ser293Pro
XM_006714137.1:c.866-37T>C XP_006714200.1:n.866-37T>C
XR_938706.1:n.1229T>C
XR_938707.1:n.1229T>C
XM_005262821.4:c.877T>C XP_005262878.1:p.Ser293Pro
XM_005262822.4:c.877T>C XP_005262879.1:p.Ser293Pro
XM_005262823.4:c.607T>C XP_005262880.1:p.Ser203Pro
XM_006714137.3:c.866-37T>C XP_006714200.1:n.866-37T>C
XM_017007884.2:c.877T>C XP_016863373.1:p.Ser293Pro
XM_017007885.2:c.877T>C XP_016863374.1:p.Ser293Pro
XM_017007886.2:c.877T>C XP_016863375.1:p.Ser293Pro
XR_001741172.2:n.1210T>C
NM_000128.4:c.877T>C MANE Select NP_000119.1:p.Ser293Pro