Canonical Allele Identifier: CA358945925

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209637C>G (hg19) ; chr4:g.186288483C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288483C>G , CM000666.2:g.186288483C>G	GRCh38
NC_000004.11:g.187209637C>G , CM000666.1:g.187209637C>G	GRCh37
NC_000004.10:g.187446631C>G	NCBI36
NG_008051.1:g.27520C>G , LRG_583:g.27520C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1747C>G (F11) MANE Select	ENSP00000384957.2:p.His583Asp
ENST00000264691.4:c.347C>G (F11)
ENST00000264692.8:c.1585C>G (F11)	ENSP00000264692.5:p.His529Asp
ENST00000403665.6:c.1747C>G (F11)	ENSP00000384957.2:p.His583Asp
ENST00000503841.1:n.266C>G (F11)
NM_000128.3:c.1747C>G , LRG_583t1:c.1747C>G (F11)	NP_000119.1:p.His583Asp
NR_033900.1:n.1011G>C (F11-AS1)
XM_005262821.2:c.1750C>G (F11)	XP_005262878.1:p.His584Asp
XM_005262822.2:c.1654C>G (F11)	XP_005262879.1:p.His552Asp
XM_005262823.2:c.1480C>G (F11)	XP_005262880.1:p.His494Asp
XM_006714137.1:c.1702C>G (F11)	XP_006714200.1:p.His568Asp
XM_005262821.4:c.1750C>G (F11)	XP_005262878.1:p.His584Asp
XM_005262822.4:c.1654C>G (F11)	XP_005262879.1:p.His552Asp
XM_005262823.4:c.1480C>G (F11)	XP_005262880.1:p.His494Asp
XM_006714137.3:c.1702C>G (F11)	XP_006714200.1:p.His568Asp
NM_000128.4:c.1747C>G (F11) MANE Select	NP_000119.1:p.His583Asp