Canonical Allele Identifier: CA2672904005

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288326-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288326A>G , CM000666.2:g.186288326A>G	GRCh38
NC_000004.11:g.187209480A>G , CM000666.1:g.187209480A>G	GRCh37
NC_000004.10:g.187446474A>G	NCBI36
NG_008051.1:g.27363A>G , LRG_583:g.27363A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1717-127A>G (F11) MANE Select	ENSP00000384957.2:n.1717-127A>G
ENST00000264691.4:c.317-127A>G (F11)
ENST00000264692.8:c.1555-127A>G (F11)	ENSP00000264692.5:n.1555-127A>G
ENST00000403665.6:c.1717-127A>G (F11)	ENSP00000384957.2:n.1717-127A>G
ENST00000503841.1:n.236-127A>G (F11)
NM_000128.3:c.1717-127A>G , LRG_583t1:c.1717-127A>G (F11)	NP_000119.1:n.1717-127A>G
NR_033900.1:n.1066+102T>C (F11-AS1)
XM_005262821.2:c.1720-127A>G (F11)	XP_005262878.1:n.1720-127A>G
XM_005262822.2:c.1624-127A>G (F11)	XP_005262879.1:n.1624-127A>G
XM_005262823.2:c.1450-127A>G (F11)	XP_005262880.1:n.1450-127A>G
XM_006714137.1:c.1672-127A>G (F11)	XP_006714200.1:n.1672-127A>G
XM_005262821.4:c.1720-127A>G (F11)	XP_005262878.1:n.1720-127A>G
XM_005262822.4:c.1624-127A>G (F11)	XP_005262879.1:n.1624-127A>G
XM_005262823.4:c.1450-127A>G (F11)	XP_005262880.1:n.1450-127A>G
XM_006714137.3:c.1672-127A>G (F11)	XP_006714200.1:n.1672-127A>G
NM_000128.4:c.1717-127A>G (F11) MANE Select	NP_000119.1:n.1717-127A>G