Canonical Allele Identifier: CA358945928

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209638A>C (hg19) ; chr4:g.186288484A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288484A>C , CM000666.2:g.186288484A>C	GRCh38
NC_000004.11:g.187209638A>C , CM000666.1:g.187209638A>C	GRCh37
NC_000004.10:g.187446632A>C	NCBI36
NG_008051.1:g.27521A>C , LRG_583:g.27521A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1748A>C (F11) MANE Select	ENSP00000384957.2:p.His583Pro
ENST00000264691.4:c.348A>C (F11)
ENST00000264692.8:c.1586A>C (F11)	ENSP00000264692.5:p.His529Pro
ENST00000403665.6:c.1748A>C (F11)	ENSP00000384957.2:p.His583Pro
ENST00000503841.1:n.267A>C (F11)
NM_000128.3:c.1748A>C , LRG_583t1:c.1748A>C (F11)	NP_000119.1:p.His583Pro
NR_033900.1:n.1010T>G (F11-AS1)
XM_005262821.2:c.1751A>C (F11)	XP_005262878.1:p.His584Pro
XM_005262822.2:c.1655A>C (F11)	XP_005262879.1:p.His552Pro
XM_005262823.2:c.1481A>C (F11)	XP_005262880.1:p.His494Pro
XM_006714137.1:c.1703A>C (F11)	XP_006714200.1:p.His568Pro
XM_005262821.4:c.1751A>C (F11)	XP_005262878.1:p.His584Pro
XM_005262822.4:c.1655A>C (F11)	XP_005262879.1:p.His552Pro
XM_005262823.4:c.1481A>C (F11)	XP_005262880.1:p.His494Pro
XM_006714137.3:c.1703A>C (F11)	XP_006714200.1:p.His568Pro
NM_000128.4:c.1748A>C (F11) MANE Select	NP_000119.1:p.His583Pro