Canonical Allele Identifier: CA1519938472
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285612C= , CM000666.2:g.186285612C= GRCh38
NC_000004.11:g.187206766C= , CM000666.1:g.187206766C= GRCh37
NC_000004.10:g.187443760C= NCBI36
NG_008051.1:g.24649C= , LRG_583:g.24649C=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1305-26C= MANE Select ENSP00000384957.2:n.1305-26C=
ENST00000264692.8:c.1143-26C= ENSP00000264692.5:n.1143-26C=
ENST00000403665.6:c.1305-26C= ENSP00000384957.2:n.1305-26C=
NM_000128.3:c.1305-26C= , LRG_583t1:c.1305-26C= NP_000119.1:n.1305-26C=
XM_005262821.2:c.1308-26C= XP_005262878.1:n.1308-26C=
XM_005262822.2:c.1308-26C= XP_005262879.1:n.1308-26C=
XM_005262823.2:c.1038-26C= XP_005262880.1:n.1038-26C=
XM_005262824.1:c.1308-26C= XP_005262881.1:n.1308-26C=
XM_006714137.1:c.1260-26C= XP_006714200.1:n.1260-26C=
XR_938706.1:n.1713-26C=
XR_938707.1:n.1713-26C=
XM_005262821.4:c.1308-26C= XP_005262878.1:n.1308-26C=
XM_005262822.4:c.1308-26C= XP_005262879.1:n.1308-26C=
XM_005262823.4:c.1038-26C= XP_005262880.1:n.1038-26C=
XM_006714137.3:c.1260-26C= XP_006714200.1:n.1260-26C=
XR_001741172.2:n.1779-26C=
NM_000128.4:c.1305-26C= MANE Select NP_000119.1:n.1305-26C=