Canonical Allele Identifier: CA358937696
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1740697838
MyVariant Identifiers: chr4:g.187201414C>A (hg19) chr4:g.186280260C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280260C>A , CM000666.2:g.186280260C>A GRCh38
NC_000004.11:g.187201414C>A , CM000666.1:g.187201414C>A GRCh37
NC_000004.10:g.187438408C>A NCBI36
NG_008051.1:g.19297C>A , LRG_583:g.19297C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.903C>A MANE Select ENSP00000384957.2:p.Phe301Leu
ENST00000264692.8:c.741C>A ENSP00000264692.5:p.Phe247Leu
ENST00000403665.6:c.903C>A ENSP00000384957.2:p.Phe301Leu
ENST00000452239.1:c.350C>A
NM_000128.3:c.903C>A , LRG_583t1:c.903C>A NP_000119.1:p.Phe301Leu
XM_005262821.2:c.903C>A XP_005262878.1:p.Phe301Leu
XM_005262822.2:c.903C>A XP_005262879.1:p.Phe301Leu
XM_005262823.2:c.633C>A XP_005262880.1:p.Phe211Leu
XM_005262824.1:c.903C>A XP_005262881.1:p.Phe301Leu
XM_006714137.1:c.866-11C>A XP_006714200.1:n.866-11C>A
XR_938706.1:n.1255C>A
XR_938707.1:n.1255C>A
XM_005262821.4:c.903C>A XP_005262878.1:p.Phe301Leu
XM_005262822.4:c.903C>A XP_005262879.1:p.Phe301Leu
XM_005262823.4:c.633C>A XP_005262880.1:p.Phe211Leu
XM_006714137.3:c.866-11C>A XP_006714200.1:n.866-11C>A
XM_017007884.2:c.903C>A XP_016863373.1:p.Phe301Leu
XM_017007885.2:c.903C>A XP_016863374.1:p.Phe301Leu
XM_017007886.2:c.903C>A XP_016863375.1:p.Phe301Leu
XR_001741172.2:n.1236C>A
NM_000128.4:c.903C>A MANE Select NP_000119.1:p.Phe301Leu
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