Canonical Allele Identifier: CA442638897
Gene: F11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187205265G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284111G>A , CM000666.2:g.186284111G>A GRCh38
NC_000004.11:g.187205265G>A , CM000666.1:g.187205265G>A GRCh37
NC_000004.10:g.187442259G>A NCBI36
NG_008051.1:g.23148G>A , LRG_583:g.23148G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1155G>A MANE Select ENSP00000384957.2:p.Lys385=
ENST00000264692.8:c.993G>A ENSP00000264692.5:p.Lys331=
ENST00000403665.6:c.1155G>A ENSP00000384957.2:p.Lys385=
NM_000128.3:c.1155G>A , LRG_583t1:c.1155G>A NP_000119.1:p.Lys385=
XM_005262821.2:c.1158G>A XP_005262878.1:p.Lys386=
XM_005262822.2:c.1158G>A XP_005262879.1:p.Lys386=
XM_005262823.2:c.888G>A XP_005262880.1:p.Lys296=
XM_005262824.1:c.1158G>A XP_005262881.1:p.Lys386=
XM_006714137.1:c.1110G>A XP_006714200.1:p.Lys370=
XR_938706.1:n.1563G>A
XR_938707.1:n.1563G>A
XM_005262821.4:c.1158G>A XP_005262878.1:p.Lys386=
XM_005262822.4:c.1158G>A XP_005262879.1:p.Lys386=
XM_005262823.4:c.888G>A XP_005262880.1:p.Lys296=
XM_006714137.3:c.1110G>A XP_006714200.1:p.Lys370=
XM_017007884.2:c.*2127G>A XP_016863373.1:n.*2127G>A
XM_017007885.2:c.*23G>A XP_016863374.1:n.*23G>A
XR_001741172.2:n.1629G>A
NM_000128.4:c.1155G>A MANE Select NP_000119.1:p.Lys385=