Canonical Allele Identifier: CA358941615
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284118A>C , CM000666.2:g.186284118A>C GRCh38
NC_000004.11:g.187205272A>C , CM000666.1:g.187205272A>C GRCh37
NC_000004.10:g.187442266A>C NCBI36
NG_008051.1:g.23155A>C , LRG_583:g.23155A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1162A>C MANE Select ENSP00000384957.2:p.Ile388Leu
ENST00000264692.8:c.1000A>C ENSP00000264692.5:p.Ile334Leu
ENST00000403665.6:c.1162A>C ENSP00000384957.2:p.Ile388Leu
NM_000128.3:c.1162A>C , LRG_583t1:c.1162A>C NP_000119.1:p.Ile388Leu
XM_005262821.2:c.1165A>C XP_005262878.1:p.Ile389Leu
XM_005262822.2:c.1165A>C XP_005262879.1:p.Ile389Leu
XM_005262823.2:c.895A>C XP_005262880.1:p.Ile299Leu
XM_005262824.1:c.1165A>C XP_005262881.1:p.Ile389Leu
XM_006714137.1:c.1117A>C XP_006714200.1:p.Ile373Leu
XR_938706.1:n.1570A>C
XR_938707.1:n.1570A>C
XM_005262821.4:c.1165A>C XP_005262878.1:p.Ile389Leu
XM_005262822.4:c.1165A>C XP_005262879.1:p.Ile389Leu
XM_005262823.4:c.895A>C XP_005262880.1:p.Ile299Leu
XM_006714137.3:c.1117A>C XP_006714200.1:p.Ile373Leu
XM_017007884.2:c.*2134A>C XP_016863373.1:n.*2134A>C
XM_017007885.2:c.*30A>C XP_016863374.1:n.*30A>C
XR_001741172.2:n.1636A>C
NM_000128.4:c.1162A>C MANE Select NP_000119.1:p.Ile388Leu