Canonical Allele Identifier: CA1519934094
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276105_186276106delinsTA , CM000666.2:g.186276105_186276106delinsTA GRCh38
NC_000004.11:g.187197259_187197260delinsTA , CM000666.1:g.187197259_187197260delinsTA GRCh37
NC_000004.10:g.187434253_187434254delinsTA NCBI36
NG_008051.1:g.15142_15143delinsTA , LRG_583:g.15142_15143delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.596-126_596-125delinsTA MANE Select ENSP00000384957.2:n.596-126_596-125delins...
ENST00000264692.8:c.434-126_434-125delinsTA ENSP00000264692.5:n.434-126_434-125delins...
ENST00000403665.6:c.596-126_596-125delinsTA ENSP00000384957.2:n.596-126_596-125delins...
ENST00000452239.1:c.43-126_43-125delinsTA
NM_000128.3:c.596-126_596-125delinsTA , LRG_583t1:c.596-126_596-125delinsTA NP_000119.1:n.596-126_596-125delinsTA
XM_005262821.2:c.596-126_596-125delinsTA XP_005262878.1:n.596-126_596-125delinsTA
XM_005262822.2:c.596-126_596-125delinsTA XP_005262879.1:n.596-126_596-125delinsTA
XM_005262823.2:c.485+1830_485+1831delinsTA XP_005262880.1:n.485+1830_485+1831delinsT...
XM_005262824.1:c.596-126_596-125delinsTA XP_005262881.1:n.596-126_596-125delinsTA
XM_006714137.1:c.596-126_596-125delinsTA XP_006714200.1:n.596-126_596-125delinsTA
XR_938706.1:n.948-126_948-125delinsTA
XR_938707.1:n.948-126_948-125delinsTA
XM_005262821.4:c.596-126_596-125delinsTA XP_005262878.1:n.596-126_596-125delinsTA
XM_005262822.4:c.596-126_596-125delinsTA XP_005262879.1:n.596-126_596-125delinsTA
XM_005262823.4:c.485+1830_485+1831delinsTA XP_005262880.1:n.485+1830_485+1831delinsT...
XM_006714137.3:c.596-126_596-125delinsTA XP_006714200.1:n.596-126_596-125delinsTA
XM_017007884.2:c.596-126_596-125delinsTA XP_016863373.1:n.596-126_596-125delinsTA
XM_017007885.2:c.596-126_596-125delinsTA XP_016863374.1:n.596-126_596-125delinsTA
XM_017007886.2:c.596-126_596-125delinsTA XP_016863375.1:n.596-126_596-125delinsTA
XR_001741172.2:n.929-126_929-125delinsTA
NM_000128.4:c.596-126_596-125delinsTA MANE Select NP_000119.1:n.596-126_596-125delinsTA