Canonical Allele Identifier: CA358945857

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288466-G-A
• MyVariant Identifiers: chr4:g.187209620G>A (hg19) ; chr4:g.186288466G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288466G>A , CM000666.2:g.186288466G>A	GRCh38
NC_000004.11:g.187209620G>A , CM000666.1:g.187209620G>A	GRCh37
NC_000004.10:g.187446614G>A	NCBI36
NG_008051.1:g.27503G>A , LRG_583:g.27503G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1730G>A (F11) MANE Select	ENSP00000384957.2:p.Gly577Asp
ENST00000264691.4:c.330G>A (F11)
ENST00000264692.8:c.1568G>A (F11)	ENSP00000264692.5:p.Gly523Asp
ENST00000403665.6:c.1730G>A (F11)	ENSP00000384957.2:p.Gly577Asp
ENST00000503841.1:n.249G>A (F11)
NM_000128.3:c.1730G>A , LRG_583t1:c.1730G>A (F11)	NP_000119.1:p.Gly577Asp
NR_033900.1:n.1028C>T (F11-AS1)
XM_005262821.2:c.1733G>A (F11)	XP_005262878.1:p.Gly578Asp
XM_005262822.2:c.1637G>A (F11)	XP_005262879.1:p.Gly546Asp
XM_005262823.2:c.1463G>A (F11)	XP_005262880.1:p.Gly488Asp
XM_006714137.1:c.1685G>A (F11)	XP_006714200.1:p.Gly562Asp
XM_005262821.4:c.1733G>A (F11)	XP_005262878.1:p.Gly578Asp
XM_005262822.4:c.1637G>A (F11)	XP_005262879.1:p.Gly546Asp
XM_005262823.4:c.1463G>A (F11)	XP_005262880.1:p.Gly488Asp
XM_006714137.3:c.1685G>A (F11)	XP_006714200.1:p.Gly562Asp
NM_000128.4:c.1730G>A (F11) MANE Select	NP_000119.1:p.Gly577Asp