Canonical Allele Identifier: CA1071938221
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1740988284

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284058T>A , CM000666.2:g.186284058T>A GRCh38
NC_000004.11:g.187205212T>A , CM000666.1:g.187205212T>A GRCh37
NC_000004.10:g.187442206T>A NCBI36
NG_008051.1:g.23095T>A , LRG_583:g.23095T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1136-34T>A MANE Select ENSP00000384957.2:n.1136-34T>A
ENST00000264692.8:c.974-34T>A ENSP00000264692.5:n.974-34T>A
ENST00000403665.6:c.1136-34T>A ENSP00000384957.2:n.1136-34T>A
NM_000128.3:c.1136-34T>A , LRG_583t1:c.1136-34T>A NP_000119.1:n.1136-34T>A
XM_005262821.2:c.1139-34T>A XP_005262878.1:n.1139-34T>A
XM_005262822.2:c.1139-34T>A XP_005262879.1:n.1139-34T>A
XM_005262823.2:c.869-34T>A XP_005262880.1:n.869-34T>A
XM_005262824.1:c.1139-34T>A XP_005262881.1:n.1139-34T>A
XM_006714137.1:c.1091-34T>A XP_006714200.1:n.1091-34T>A
XR_938706.1:n.1544-34T>A
XR_938707.1:n.1544-34T>A
XM_005262821.4:c.1139-34T>A XP_005262878.1:n.1139-34T>A
XM_005262822.4:c.1139-34T>A XP_005262879.1:n.1139-34T>A
XM_005262823.4:c.869-34T>A XP_005262880.1:n.869-34T>A
XM_006714137.3:c.1091-34T>A XP_006714200.1:n.1091-34T>A
XM_017007884.2:c.*2074T>A XP_016863373.1:n.*2074T>A
XM_017007885.2:c.*4-34T>A XP_016863374.1:n.*4-34T>A
XR_001741172.2:n.1610-34T>A
NM_000128.4:c.1136-34T>A MANE Select NP_000119.1:n.1136-34T>A