Canonical Allele Identifier: CA358941613
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1162A>T MANE Select ENSP00000384957.2:p.Ile388Phe
ENST00000264692.8:c.1000A>T ENSP00000264692.5:p.Ile334Phe
ENST00000403665.6:c.1162A>T ENSP00000384957.2:p.Ile388Phe
NM_000128.3:c.1162A>T , LRG_583t1:c.1162A>T NP_000119.1:p.Ile388Phe
XM_005262821.2:c.1165A>T XP_005262878.1:p.Ile389Phe
XM_005262822.2:c.1165A>T XP_005262879.1:p.Ile389Phe
XM_005262823.2:c.895A>T XP_005262880.1:p.Ile299Phe
XM_005262824.1:c.1165A>T XP_005262881.1:p.Ile389Phe
XM_006714137.1:c.1117A>T XP_006714200.1:p.Ile373Phe
XR_938706.1:n.1570A>T
XR_938707.1:n.1570A>T
XM_005262821.4:c.1165A>T XP_005262878.1:p.Ile389Phe
XM_005262822.4:c.1165A>T XP_005262879.1:p.Ile389Phe
XM_005262823.4:c.895A>T XP_005262880.1:p.Ile299Phe
XM_006714137.3:c.1117A>T XP_006714200.1:p.Ile373Phe
XM_017007884.2:c.*2134A>T XP_016863373.1:n.*2134A>T
XM_017007885.2:c.*30A>T XP_016863374.1:n.*30A>T
XR_001741172.2:n.1636A>T
NM_000128.4:c.1162A>T MANE Select NP_000119.1:p.Ile388Phe