Canonical Allele Identifier: CA2672903604

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186286606-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286606C>T , CM000666.2:g.186286606C>T	GRCh38
NC_000004.11:g.187207760C>T , CM000666.1:g.187207760C>T	GRCh37
NC_000004.10:g.187444754C>T	NCBI36
NG_008051.1:g.25643C>T , LRG_583:g.25643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1576+96C>T (F11) MANE Select	ENSP00000384957.2:n.1576+96C>T
ENST00000264691.4:c.176+793C>T (F11)
ENST00000264692.8:c.1414+96C>T (F11)	ENSP00000264692.5:n.1414+96C>T
ENST00000403665.6:c.1576+96C>T (F11)	ENSP00000384957.2:n.1576+96C>T
NM_000128.3:c.1576+96C>T , LRG_583t1:c.1576+96C>T (F11)	NP_000119.1:n.1576+96C>T
NR_033900.1:n.1067-340G>A (F11-AS1)
XM_005262821.2:c.1579+96C>T (F11)	XP_005262878.1:n.1579+96C>T
XM_005262822.2:c.1483+793C>T (F11)	XP_005262879.1:n.1483+793C>T
XM_005262823.2:c.1309+96C>T (F11)	XP_005262880.1:n.1309+96C>T
XM_005262824.1:c.1544C>T (F11)	XP_005262881.1:p.Ser515Leu
XM_006714137.1:c.1531+96C>T (F11)	XP_006714200.1:n.1531+96C>T
XR_938706.1:n.1984+96C>T (F11)
XR_938707.1:n.1888+793C>T (F11)
XM_005262821.4:c.1579+96C>T (F11)	XP_005262878.1:n.1579+96C>T
XM_005262822.4:c.1483+793C>T (F11)	XP_005262879.1:n.1483+793C>T
XM_005262823.4:c.1309+96C>T (F11)	XP_005262880.1:n.1309+96C>T
XM_006714137.3:c.1531+96C>T (F11)	XP_006714200.1:n.1531+96C>T
NM_000128.4:c.1576+96C>T (F11) MANE Select	NP_000119.1:n.1576+96C>T