Canonical Allele Identifier: CA358945729

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287811G>T , CM000666.2:g.186287811G>T GRCh38
NC_000004.11:g.187208965G>T , CM000666.1:g.187208965G>T GRCh37
NC_000004.10:g.187445959G>T NCBI36
NG_008051.1:g.26848G>T , LRG_583:g.26848G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1704G>T (F11) MANE Select ENSP00000384957.2:p.Lys568Asn
ENST00000264691.4:c.304G>T (F11)
ENST00000264692.8:c.1542G>T (F11) ENSP00000264692.5:p.Lys514Asn
ENST00000403665.6:c.1704G>T (F11) ENSP00000384957.2:p.Lys568Asn
ENST00000503841.1:n.223G>T (F11)
NM_000128.3:c.1704G>T , LRG_583t1:c.1704G>T (F11) NP_000119.1:p.Lys568Asn
NR_033900.1:n.1066+617C>A (F11-AS1)
XM_005262821.2:c.1707G>T (F11) XP_005262878.1:p.Lys569Asn
XM_005262822.2:c.1611G>T (F11) XP_005262879.1:p.Lys537Asn
XM_005262823.2:c.1437G>T (F11) XP_005262880.1:p.Lys479Asn
XM_006714137.1:c.1659G>T (F11) XP_006714200.1:p.Lys553Asn
XM_005262821.4:c.1707G>T (F11) XP_005262878.1:p.Lys569Asn
XM_005262822.4:c.1611G>T (F11) XP_005262879.1:p.Lys537Asn
XM_005262823.4:c.1437G>T (F11) XP_005262880.1:p.Lys479Asn
XM_006714137.3:c.1659G>T (F11) XP_006714200.1:p.Lys553Asn
NM_000128.4:c.1704G>T (F11) MANE Select NP_000119.1:p.Lys568Asn