Canonical Allele Identifier: CA358937600
Gene: F11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187201398A>G (hg19) chr4:g.186280244A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280244A>G , CM000666.2:g.186280244A>G GRCh38
NC_000004.11:g.187201398A>G , CM000666.1:g.187201398A>G GRCh37
NC_000004.10:g.187438392A>G NCBI36
NG_008051.1:g.19281A>G , LRG_583:g.19281A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.887A>G MANE Select ENSP00000384957.2:p.Tyr296Cys
ENST00000264692.8:c.725A>G ENSP00000264692.5:p.Tyr242Cys
ENST00000403665.6:c.887A>G ENSP00000384957.2:p.Tyr296Cys
ENST00000452239.1:c.334A>G
NM_000128.3:c.887A>G , LRG_583t1:c.887A>G NP_000119.1:p.Tyr296Cys
XM_005262821.2:c.887A>G XP_005262878.1:p.Tyr296Cys
XM_005262822.2:c.887A>G XP_005262879.1:p.Tyr296Cys
XM_005262823.2:c.617A>G XP_005262880.1:p.Tyr206Cys
XM_005262824.1:c.887A>G XP_005262881.1:p.Tyr296Cys
XM_006714137.1:c.866-27A>G XP_006714200.1:n.866-27A>G
XR_938706.1:n.1239A>G
XR_938707.1:n.1239A>G
XM_005262821.4:c.887A>G XP_005262878.1:p.Tyr296Cys
XM_005262822.4:c.887A>G XP_005262879.1:p.Tyr296Cys
XM_005262823.4:c.617A>G XP_005262880.1:p.Tyr206Cys
XM_006714137.3:c.866-27A>G XP_006714200.1:n.866-27A>G
XM_017007884.2:c.887A>G XP_016863373.1:p.Tyr296Cys
XM_017007885.2:c.887A>G XP_016863374.1:p.Tyr296Cys
XM_017007886.2:c.887A>G XP_016863375.1:p.Tyr296Cys
XR_001741172.2:n.1220A>G
NM_000128.4:c.887A>G MANE Select NP_000119.1:p.Tyr296Cys
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