Canonical Allele Identifier: CA358941580
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1155G>C MANE Select ENSP00000384957.2:p.Lys385Asn
ENST00000264692.8:c.993G>C ENSP00000264692.5:p.Lys331Asn
ENST00000403665.6:c.1155G>C ENSP00000384957.2:p.Lys385Asn
NM_000128.3:c.1155G>C , LRG_583t1:c.1155G>C NP_000119.1:p.Lys385Asn
XM_005262821.2:c.1158G>C XP_005262878.1:p.Lys386Asn
XM_005262822.2:c.1158G>C XP_005262879.1:p.Lys386Asn
XM_005262823.2:c.888G>C XP_005262880.1:p.Lys296Asn
XM_005262824.1:c.1158G>C XP_005262881.1:p.Lys386Asn
XM_006714137.1:c.1110G>C XP_006714200.1:p.Lys370Asn
XR_938706.1:n.1563G>C
XR_938707.1:n.1563G>C
XM_005262821.4:c.1158G>C XP_005262878.1:p.Lys386Asn
XM_005262822.4:c.1158G>C XP_005262879.1:p.Lys386Asn
XM_005262823.4:c.888G>C XP_005262880.1:p.Lys296Asn
XM_006714137.3:c.1110G>C XP_006714200.1:p.Lys370Asn
XM_017007884.2:c.*2127G>C XP_016863373.1:n.*2127G>C
XM_017007885.2:c.*23G>C XP_016863374.1:n.*23G>C
XR_001741172.2:n.1629G>C
NM_000128.4:c.1155G>C MANE Select NP_000119.1:p.Lys385Asn