Canonical Allele Identifier: CA1519937770
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284162G= , CM000666.2:g.186284162G= GRCh38
NC_000004.11:g.187205316G= , CM000666.1:g.187205316G= GRCh37
NC_000004.10:g.187442310G= NCBI36
NG_008051.1:g.23199G= , LRG_583:g.23199G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1206G= MANE Select ENSP00000384957.2:p.Gln402=
ENST00000264692.8:c.1044G= ENSP00000264692.5:p.Gln348=
ENST00000403665.6:c.1206G= ENSP00000384957.2:p.Gln402=
NM_000128.3:c.1206G= , LRG_583t1:c.1206G= NP_000119.1:p.Gln402=
XM_005262821.2:c.1209G= XP_005262878.1:p.Gln403=
XM_005262822.2:c.1209G= XP_005262879.1:p.Gln403=
XM_005262823.2:c.939G= XP_005262880.1:p.Gln313=
XM_005262824.1:c.1209G= XP_005262881.1:p.Gln403=
XM_006714137.1:c.1161G= XP_006714200.1:p.Gln387=
XR_938706.1:n.1614G=
XR_938707.1:n.1614G=
XM_005262821.4:c.1209G= XP_005262878.1:p.Gln403=
XM_005262822.4:c.1209G= XP_005262879.1:p.Gln403=
XM_005262823.4:c.939G= XP_005262880.1:p.Gln313=
XM_006714137.3:c.1161G= XP_006714200.1:p.Gln387=
XM_017007884.2:c.*2178G= XP_016863373.1:n.*2178G=
XM_017007885.2:c.*74G= XP_016863374.1:n.*74G=
XR_001741172.2:n.1680G=
NM_000128.4:c.1206G= MANE Select NP_000119.1:p.Gln402=