Canonical Allele Identifier: CA442640459

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187207286T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286132T>A , CM000666.2:g.186286132T>A	GRCh38
NC_000004.11:g.187207286T>A , CM000666.1:g.187207286T>A	GRCh37
NC_000004.10:g.187444280T>A	NCBI36
NG_008051.1:g.25169T>A , LRG_583:g.25169T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1481-283T>A (F11) MANE Select	ENSP00000384957.2:n.1481-283T>A
ENST00000264691.4:c.176+319T>A (F11)
ENST00000264692.8:c.1319-283T>A (F11)	ENSP00000264692.5:n.1319-283T>A
ENST00000403665.6:c.1481-283T>A (F11)	ENSP00000384957.2:n.1481-283T>A
NM_000128.3:c.1481-283T>A , LRG_583t1:c.1481-283T>A (F11)	NP_000119.1:n.1481-283T>A
NR_033900.1:n.1201A>T (F11-AS1)
XM_005262821.2:c.1484-283T>A (F11)	XP_005262878.1:n.1484-283T>A
XM_005262822.2:c.1483+319T>A (F11)	XP_005262879.1:n.1483+319T>A
XM_005262823.2:c.1214-283T>A (F11)	XP_005262880.1:n.1214-283T>A
XM_005262824.1:c.1483+319T>A (F11)	XP_005262881.1:n.1483+319T>A
XM_006714137.1:c.1436-283T>A (F11)	XP_006714200.1:n.1436-283T>A
XR_938706.1:n.1889-283T>A (F11)
XR_938707.1:n.1888+319T>A (F11)
XM_005262821.4:c.1484-283T>A (F11)	XP_005262878.1:n.1484-283T>A
XM_005262822.4:c.1483+319T>A (F11)	XP_005262879.1:n.1483+319T>A
XM_005262823.4:c.1214-283T>A (F11)	XP_005262880.1:n.1214-283T>A
XM_006714137.3:c.1436-283T>A (F11)	XP_006714200.1:n.1436-283T>A
XR_001741172.2:n.1955-283T>A (F11)
NM_000128.4:c.1481-283T>A (F11) MANE Select	NP_000119.1:n.1481-283T>A