Canonical Allele Identifier: CA2544466424
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280313_186280314insTGCAG , CM000666.2:g.186280313_186280314insTGCAG GRCh38
NC_000004.11:g.187201467_187201468insTGCAG , CM000666.1:g.187201467_187201468insTGCAG GRCh37
NC_000004.10:g.187438461_187438462insTGCAG NCBI36
NG_008051.1:g.19350_19351insTGCAG , LRG_583:g.19350_19351insTGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.956_957insTGCAG MANE Select ENSP00000384957.2:p.Lys319AsnfsTer32
ENST00000264692.8:c.794_795insTGCAG ENSP00000264692.5:p.Lys265AsnfsTer32
ENST00000403665.6:c.956_957insTGCAG ENSP00000384957.2:p.Lys319AsnfsTer32
ENST00000452239.1:c.403_404insTGCAG
NM_000128.3:c.956_957insTGCAG , LRG_583t1:c.956_957insTGCAG NP_000119.1:p.Lys319AsnfsTer32
XM_005262821.2:c.956_957insTGCAG XP_005262878.1:p.Lys319AsnfsTer?
XM_005262822.2:c.956_957insTGCAG XP_005262879.1:p.Lys319AsnfsTer?
XM_005262823.2:c.686_687insTGCAG XP_005262880.1:p.Lys229AsnfsTer?
XM_005262824.1:c.956_957insTGCAG XP_005262881.1:p.Lys319AsnfsTer?
XM_006714137.1:c.908_909insTGCAG XP_006714200.1:p.Lys303AsnfsTer?
XR_938706.1:n.1308_1309insTGCAG
XR_938707.1:n.1308_1309insTGCAG
XM_005262821.4:c.956_957insTGCAG XP_005262878.1:p.Lys319AsnfsTer?
XM_005262822.4:c.956_957insTGCAG XP_005262879.1:p.Lys319AsnfsTer?
XM_005262823.4:c.686_687insTGCAG XP_005262880.1:p.Lys229AsnfsTer?
XM_006714137.3:c.908_909insTGCAG XP_006714200.1:p.Lys303AsnfsTer?
XM_017007884.2:c.956_957insTGCAG XP_016863373.1:p.Lys319AsnfsTer?
XM_017007885.2:c.956_957insTGCAG XP_016863374.1:p.Lys319AsnfsTer?
XM_017007886.2:c.956_957insTGCAG XP_016863375.1:p.Lys319AsnfsTer32
XR_001741172.2:n.1289_1290insTGCAG
NM_000128.4:c.956_957insTGCAG MANE Select NP_000119.1:p.Lys319AsnfsTer32