Canonical Allele Identifier: CA358941588
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs756583258

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284113C>A , CM000666.2:g.186284113C>A GRCh38
NC_000004.11:g.187205267C>A , CM000666.1:g.187205267C>A GRCh37
NC_000004.10:g.187442261C>A NCBI36
NG_008051.1:g.23150C>A , LRG_583:g.23150C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1157C>A MANE Select ENSP00000384957.2:p.Pro386His
ENST00000264692.8:c.995C>A ENSP00000264692.5:p.Pro332His
ENST00000403665.6:c.1157C>A ENSP00000384957.2:p.Pro386His
NM_000128.3:c.1157C>A , LRG_583t1:c.1157C>A NP_000119.1:p.Pro386His
XM_005262821.2:c.1160C>A XP_005262878.1:p.Pro387His
XM_005262822.2:c.1160C>A XP_005262879.1:p.Pro387His
XM_005262823.2:c.890C>A XP_005262880.1:p.Pro297His
XM_005262824.1:c.1160C>A XP_005262881.1:p.Pro387His
XM_006714137.1:c.1112C>A XP_006714200.1:p.Pro371His
XR_938706.1:n.1565C>A
XR_938707.1:n.1565C>A
XM_005262821.4:c.1160C>A XP_005262878.1:p.Pro387His
XM_005262822.4:c.1160C>A XP_005262879.1:p.Pro387His
XM_005262823.4:c.890C>A XP_005262880.1:p.Pro297His
XM_006714137.3:c.1112C>A XP_006714200.1:p.Pro371His
XM_017007884.2:c.*2129C>A XP_016863373.1:n.*2129C>A
XM_017007885.2:c.*25C>A XP_016863374.1:n.*25C>A
XR_001741172.2:n.1631C>A
NM_000128.4:c.1157C>A MANE Select NP_000119.1:p.Pro386His