Canonical Allele Identifier: CA913103789
Gene: F11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187201495dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280341dup , CM000666.2:g.186280341dup GRCh38
NC_000004.11:g.187201495dup , CM000666.1:g.187201495dup GRCh37
NC_000004.10:g.187438489dup NCBI36
NG_008051.1:g.19378dup , LRG_583:g.19378dup

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.984dup MANE Select ENSP00000384957.2:p.Phe329ValfsTer30
ENST00000264692.8:c.822dup ENSP00000264692.5:p.Phe275ValfsTer30
ENST00000403665.6:c.984dup ENSP00000384957.2:p.Phe329ValfsTer30
ENST00000452239.1:c.431dup
NM_000128.3:c.984dup , LRG_583t1:c.984dup NP_000119.1:p.Phe329ValfsTer30
XM_005262821.2:c.984dup XP_005262878.1:p.Phe329ValfsTer?
XM_005262822.2:c.984dup XP_005262879.1:p.Phe329ValfsTer?
XM_005262823.2:c.714dup XP_005262880.1:p.Phe239ValfsTer?
XM_005262824.1:c.984dup XP_005262881.1:p.Phe329ValfsTer?
XM_006714137.1:c.936dup XP_006714200.1:p.Phe313ValfsTer?
XR_938706.1:n.1336dup
XR_938707.1:n.1336dup
XM_005262821.4:c.984dup XP_005262878.1:p.Phe329ValfsTer?
XM_005262822.4:c.984dup XP_005262879.1:p.Phe329ValfsTer?
XM_005262823.4:c.714dup XP_005262880.1:p.Phe239ValfsTer?
XM_006714137.3:c.936dup XP_006714200.1:p.Phe313ValfsTer?
XM_017007884.2:c.984dup XP_016863373.1:p.Phe329ValfsTer?
XM_017007885.2:c.984dup XP_016863374.1:p.Phe329ValfsTer?
XM_017007886.2:c.984dup XP_016863375.1:p.Phe329ValfsTer30
XR_001741172.2:n.1317dup
NM_000128.4:c.984dup MANE Select NP_000119.1:p.Phe329ValfsTer30