Canonical Allele Identifier: CA1519938448
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285564G= , CM000666.2:g.186285564G= GRCh38
NC_000004.11:g.187206718G= , CM000666.1:g.187206718G= GRCh37
NC_000004.10:g.187443712G= NCBI36
NG_008051.1:g.24601G= , LRG_583:g.24601G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1305-74G= MANE Select ENSP00000384957.2:n.1305-74G=
ENST00000264692.8:c.1143-74G= ENSP00000264692.5:n.1143-74G=
ENST00000403665.6:c.1305-74G= ENSP00000384957.2:n.1305-74G=
NM_000128.3:c.1305-74G= , LRG_583t1:c.1305-74G= NP_000119.1:n.1305-74G=
XM_005262821.2:c.1308-74G= XP_005262878.1:n.1308-74G=
XM_005262822.2:c.1308-74G= XP_005262879.1:n.1308-74G=
XM_005262823.2:c.1038-74G= XP_005262880.1:n.1038-74G=
XM_005262824.1:c.1308-74G= XP_005262881.1:n.1308-74G=
XM_006714137.1:c.1260-74G= XP_006714200.1:n.1260-74G=
XR_938706.1:n.1713-74G=
XR_938707.1:n.1713-74G=
XM_005262821.4:c.1308-74G= XP_005262878.1:n.1308-74G=
XM_005262822.4:c.1308-74G= XP_005262879.1:n.1308-74G=
XM_005262823.4:c.1038-74G= XP_005262880.1:n.1038-74G=
XM_006714137.3:c.1260-74G= XP_006714200.1:n.1260-74G=
XR_001741172.2:n.1779-74G=
NM_000128.4:c.1305-74G= MANE Select NP_000119.1:n.1305-74G=