Canonical Allele Identifier: CA112106083

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1012510296
• gnomAD v3: 4-186288419-T-A
• gnomAD v4: 4-186288419-T-A
• MyVariant Identifiers: chr4:g.187209573T>A (hg19) ; chr4:g.186288419T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288419T>A , CM000666.2:g.186288419T>A	GRCh38
NC_000004.11:g.187209573T>A , CM000666.1:g.187209573T>A	GRCh37
NC_000004.10:g.187446567T>A	NCBI36
NG_008051.1:g.27456T>A , LRG_583:g.27456T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1717-34T>A (F11) MANE Select	ENSP00000384957.2:n.1717-34T>A
ENST00000264691.4:c.317-34T>A (F11)
ENST00000264692.8:c.1555-34T>A (F11)	ENSP00000264692.5:n.1555-34T>A
ENST00000403665.6:c.1717-34T>A (F11)	ENSP00000384957.2:n.1717-34T>A
ENST00000503841.1:n.236-34T>A (F11)
NM_000128.3:c.1717-34T>A , LRG_583t1:c.1717-34T>A (F11)	NP_000119.1:n.1717-34T>A
NR_033900.1:n.1066+9A>T (F11-AS1)
XM_005262821.2:c.1720-34T>A (F11)	XP_005262878.1:n.1720-34T>A
XM_005262822.2:c.1624-34T>A (F11)	XP_005262879.1:n.1624-34T>A
XM_005262823.2:c.1450-34T>A (F11)	XP_005262880.1:n.1450-34T>A
XM_006714137.1:c.1672-34T>A (F11)	XP_006714200.1:n.1672-34T>A
XM_005262821.4:c.1720-34T>A (F11)	XP_005262878.1:n.1720-34T>A
XM_005262822.4:c.1624-34T>A (F11)	XP_005262879.1:n.1624-34T>A
XM_005262823.4:c.1450-34T>A (F11)	XP_005262880.1:n.1450-34T>A
XM_006714137.3:c.1672-34T>A (F11)	XP_006714200.1:n.1672-34T>A
NM_000128.4:c.1717-34T>A (F11) MANE Select	NP_000119.1:n.1717-34T>A