Canonical Allele Identifier: CA1519938513
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285707A= , CM000666.2:g.186285707A= GRCh38
NC_000004.11:g.187206861A= , CM000666.1:g.187206861A= GRCh37
NC_000004.10:g.187443855A= NCBI36
NG_008051.1:g.24744A= , LRG_583:g.24744A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1374A= MANE Select ENSP00000384957.2:p.Thr458=
ENST00000264691.4:c.70A=
ENST00000264692.8:c.1212A= ENSP00000264692.5:p.Thr404=
ENST00000403665.6:c.1374A= ENSP00000384957.2:p.Thr458=
NM_000128.3:c.1374A= , LRG_583t1:c.1374A= NP_000119.1:p.Thr458=
XM_005262821.2:c.1377A= XP_005262878.1:p.Thr459=
XM_005262822.2:c.1377A= XP_005262879.1:p.Thr459=
XM_005262823.2:c.1107A= XP_005262880.1:p.Thr369=
XM_005262824.1:c.1377A= XP_005262881.1:p.Thr459=
XM_006714137.1:c.1329A= XP_006714200.1:p.Thr443=
XR_938706.1:n.1782A=
XR_938707.1:n.1782A=
XM_005262821.4:c.1377A= XP_005262878.1:p.Thr459=
XM_005262822.4:c.1377A= XP_005262879.1:p.Thr459=
XM_005262823.4:c.1107A= XP_005262880.1:p.Thr369=
XM_006714137.3:c.1329A= XP_006714200.1:p.Thr443=
XR_001741172.2:n.1848A=
NM_000128.4:c.1374A= MANE Select NP_000119.1:p.Thr458=