Canonical Allele Identifier: CA1519937719
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284070C= , CM000666.2:g.186284070C= GRCh38
NC_000004.11:g.187205224C= , CM000666.1:g.187205224C= GRCh37
NC_000004.10:g.187442218C= NCBI36
NG_008051.1:g.23107C= , LRG_583:g.23107C=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1136-22C= MANE Select ENSP00000384957.2:n.1136-22C=
ENST00000264692.8:c.974-22C= ENSP00000264692.5:n.974-22C=
ENST00000403665.6:c.1136-22C= ENSP00000384957.2:n.1136-22C=
NM_000128.3:c.1136-22C= , LRG_583t1:c.1136-22C= NP_000119.1:n.1136-22C=
XM_005262821.2:c.1139-22C= XP_005262878.1:n.1139-22C=
XM_005262822.2:c.1139-22C= XP_005262879.1:n.1139-22C=
XM_005262823.2:c.869-22C= XP_005262880.1:n.869-22C=
XM_005262824.1:c.1139-22C= XP_005262881.1:n.1139-22C=
XM_006714137.1:c.1091-22C= XP_006714200.1:n.1091-22C=
XR_938706.1:n.1544-22C=
XR_938707.1:n.1544-22C=
XM_005262821.4:c.1139-22C= XP_005262878.1:n.1139-22C=
XM_005262822.4:c.1139-22C= XP_005262879.1:n.1139-22C=
XM_005262823.4:c.869-22C= XP_005262880.1:n.869-22C=
XM_006714137.3:c.1091-22C= XP_006714200.1:n.1091-22C=
XM_017007884.2:c.*2086C= XP_016863373.1:n.*2086C=
XM_017007885.2:c.*4-22C= XP_016863374.1:n.*4-22C=
XR_001741172.2:n.1610-22C=
NM_000128.4:c.1136-22C= MANE Select NP_000119.1:n.1136-22C=