Canonical Allele Identifier: CA358944149

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187207619T>G (hg19) ; chr4:g.186286465T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286465T>G , CM000666.2:g.186286465T>G	GRCh38
NC_000004.11:g.187207619T>G , CM000666.1:g.187207619T>G	GRCh37
NC_000004.10:g.187444613T>G	NCBI36
NG_008051.1:g.25502T>G , LRG_583:g.25502T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1531T>G (F11) MANE Select	ENSP00000384957.2:p.Tyr511Asp
ENST00000264691.4:c.176+652T>G (F11)
ENST00000264692.8:c.1369T>G (F11)	ENSP00000264692.5:p.Tyr457Asp
ENST00000403665.6:c.1531T>G (F11)	ENSP00000384957.2:p.Tyr511Asp
NM_000128.3:c.1531T>G , LRG_583t1:c.1531T>G (F11)	NP_000119.1:p.Tyr511Asp
NR_033900.1:n.1067-199A>C (F11-AS1)
XM_005262821.2:c.1534T>G (F11)	XP_005262878.1:p.Tyr512Asp
XM_005262822.2:c.1483+652T>G (F11)	XP_005262879.1:n.1483+652T>G
XM_005262823.2:c.1264T>G (F11)	XP_005262880.1:p.Tyr422Asp
XM_005262824.1:c.1484-81T>G (F11)	XP_005262881.1:n.1484-81T>G
XM_006714137.1:c.1486T>G (F11)	XP_006714200.1:p.Tyr496Asp
XR_938706.1:n.1939T>G (F11)
XR_938707.1:n.1888+652T>G (F11)
XM_005262821.4:c.1534T>G (F11)	XP_005262878.1:p.Tyr512Asp
XM_005262822.4:c.1483+652T>G (F11)	XP_005262879.1:n.1483+652T>G
XM_005262823.4:c.1264T>G (F11)	XP_005262880.1:p.Tyr422Asp
XM_006714137.3:c.1486T>G (F11)	XP_006714200.1:p.Tyr496Asp
XR_001741172.2:n.2005T>G (F11)
NM_000128.4:c.1531T>G (F11) MANE Select	NP_000119.1:p.Tyr511Asp