Canonical Allele Identifier: CA2672903846

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186287594-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287594A>G , CM000666.2:g.186287594A>G	GRCh38
NC_000004.11:g.187208748A>G , CM000666.1:g.187208748A>G	GRCh37
NC_000004.10:g.187445742A>G	NCBI36
NG_008051.1:g.26631A>G , LRG_583:g.26631A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1577-90A>G (F11) MANE Select	ENSP00000384957.2:n.1577-90A>G
ENST00000264691.4:c.177-90A>G (F11)
ENST00000264692.8:c.1415-90A>G (F11)	ENSP00000264692.5:n.1415-90A>G
ENST00000403665.6:c.1577-90A>G (F11)	ENSP00000384957.2:n.1577-90A>G
ENST00000503841.1:n.6A>G (F11)
NM_000128.3:c.1577-90A>G , LRG_583t1:c.1577-90A>G (F11)	NP_000119.1:n.1577-90A>G
NR_033900.1:n.1066+834T>C (F11-AS1)
XM_005262821.2:c.1580-90A>G (F11)	XP_005262878.1:n.1580-90A>G
XM_005262822.2:c.1484-90A>G (F11)	XP_005262879.1:n.1484-90A>G
XM_005262823.2:c.1310-90A>G (F11)	XP_005262880.1:n.1310-90A>G
XM_006714137.1:c.1532-90A>G (F11)	XP_006714200.1:n.1532-90A>G
XR_938706.1:n.1985-90A>G (F11)
XR_938707.1:n.1889-90A>G (F11)
XM_005262821.4:c.1580-90A>G (F11)	XP_005262878.1:n.1580-90A>G
XM_005262822.4:c.1484-90A>G (F11)	XP_005262879.1:n.1484-90A>G
XM_005262823.4:c.1310-90A>G (F11)	XP_005262880.1:n.1310-90A>G
XM_006714137.3:c.1532-90A>G (F11)	XP_006714200.1:n.1532-90A>G
NM_000128.4:c.1577-90A>G (F11) MANE Select	NP_000119.1:n.1577-90A>G