Canonical Allele Identifier: CA1519937711
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284064G= , CM000666.2:g.186284064G= GRCh38
NC_000004.11:g.187205218G= , CM000666.1:g.187205218G= GRCh37
NC_000004.10:g.187442212G= NCBI36
NG_008051.1:g.23101G= , LRG_583:g.23101G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1136-28G= MANE Select ENSP00000384957.2:n.1136-28G=
ENST00000264692.8:c.974-28G= ENSP00000264692.5:n.974-28G=
ENST00000403665.6:c.1136-28G= ENSP00000384957.2:n.1136-28G=
NM_000128.3:c.1136-28G= , LRG_583t1:c.1136-28G= NP_000119.1:n.1136-28G=
XM_005262821.2:c.1139-28G= XP_005262878.1:n.1139-28G=
XM_005262822.2:c.1139-28G= XP_005262879.1:n.1139-28G=
XM_005262823.2:c.869-28G= XP_005262880.1:n.869-28G=
XM_005262824.1:c.1139-28G= XP_005262881.1:n.1139-28G=
XM_006714137.1:c.1091-28G= XP_006714200.1:n.1091-28G=
XR_938706.1:n.1544-28G=
XR_938707.1:n.1544-28G=
XM_005262821.4:c.1139-28G= XP_005262878.1:n.1139-28G=
XM_005262822.4:c.1139-28G= XP_005262879.1:n.1139-28G=
XM_005262823.4:c.869-28G= XP_005262880.1:n.869-28G=
XM_006714137.3:c.1091-28G= XP_006714200.1:n.1091-28G=
XM_017007884.2:c.*2080G= XP_016863373.1:n.*2080G=
XM_017007885.2:c.*4-28G= XP_016863374.1:n.*4-28G=
XR_001741172.2:n.1610-28G=
NM_000128.4:c.1136-28G= MANE Select NP_000119.1:n.1136-28G=