Canonical Allele Identifier: CA1519934188
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276308G= , CM000666.2:g.186276308G= GRCh38
NC_000004.11:g.187197462G= , CM000666.1:g.187197462G= GRCh37
NC_000004.10:g.187434456G= NCBI36
NG_008051.1:g.15345G= , LRG_583:g.15345G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.673G= MANE Select ENSP00000384957.2:p.Val225=
ENST00000264692.8:c.511G= ENSP00000264692.5:p.Val171=
ENST00000403665.6:c.673G= ENSP00000384957.2:p.Val225=
ENST00000452239.1:c.120G=
NM_000128.3:c.673G= , LRG_583t1:c.673G= NP_000119.1:p.Val225=
XM_005262821.2:c.673G= XP_005262878.1:p.Val225=
XM_005262822.2:c.673G= XP_005262879.1:p.Val225=
XM_005262823.2:c.485+2033G= XP_005262880.1:n.485+2033G=
XM_005262824.1:c.673G= XP_005262881.1:p.Val225=
XM_006714137.1:c.673G= XP_006714200.1:p.Val225=
XR_938706.1:n.1025G=
XR_938707.1:n.1025G=
XM_005262821.4:c.673G= XP_005262878.1:p.Val225=
XM_005262822.4:c.673G= XP_005262879.1:p.Val225=
XM_005262823.4:c.485+2033G= XP_005262880.1:n.485+2033G=
XM_006714137.3:c.673G= XP_006714200.1:p.Val225=
XM_017007884.2:c.673G= XP_016863373.1:p.Val225=
XM_017007885.2:c.673G= XP_016863374.1:p.Val225=
XM_017007886.2:c.673G= XP_016863375.1:p.Val225=
XR_001741172.2:n.1006G=
NM_000128.4:c.673G= MANE Select NP_000119.1:p.Val225=