Canonical Allele Identifier: CA557396142

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1230742988
• gnomAD v2: 4-187207678-T-G
• MyVariant Identifiers: chr4:g.187207678T>G (hg19) ; chr4:g.186286524T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286524T>G , CM000666.2:g.186286524T>G	GRCh38
NC_000004.11:g.187207678T>G , CM000666.1:g.187207678T>G	GRCh37
NC_000004.10:g.187444672T>G	NCBI36
NG_008051.1:g.25561T>G , LRG_583:g.25561T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1576+14T>G (F11) MANE Select	ENSP00000384957.2:n.1576+14T>G
ENST00000264691.4:c.176+711T>G (F11)
ENST00000264692.8:c.1414+14T>G (F11)	ENSP00000264692.5:n.1414+14T>G
ENST00000403665.6:c.1576+14T>G (F11)	ENSP00000384957.2:n.1576+14T>G
NM_000128.3:c.1576+14T>G , LRG_583t1:c.1576+14T>G (F11)	NP_000119.1:n.1576+14T>G
NR_033900.1:n.1067-258A>C (F11-AS1)
XM_005262821.2:c.1579+14T>G (F11)	XP_005262878.1:n.1579+14T>G
XM_005262822.2:c.1483+711T>G (F11)	XP_005262879.1:n.1483+711T>G
XM_005262823.2:c.1309+14T>G (F11)	XP_005262880.1:n.1309+14T>G
XM_005262824.1:c.1484-22T>G (F11)	XP_005262881.1:n.1484-22T>G
XM_006714137.1:c.1531+14T>G (F11)	XP_006714200.1:n.1531+14T>G
XR_938706.1:n.1984+14T>G (F11)
XR_938707.1:n.1888+711T>G (F11)
XM_005262821.4:c.1579+14T>G (F11)	XP_005262878.1:n.1579+14T>G
XM_005262822.4:c.1483+711T>G (F11)	XP_005262879.1:n.1483+711T>G
XM_005262823.4:c.1309+14T>G (F11)	XP_005262880.1:n.1309+14T>G
XM_006714137.3:c.1531+14T>G (F11)	XP_006714200.1:n.1531+14T>G
NM_000128.4:c.1576+14T>G (F11) MANE Select	NP_000119.1:n.1576+14T>G