Canonical Allele Identifier: CA358945586

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208901A>T (hg19) ; chr4:g.186287747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287747A>T , CM000666.2:g.186287747A>T	GRCh38
NC_000004.11:g.187208901A>T , CM000666.1:g.187208901A>T	GRCh37
NC_000004.10:g.187445895A>T	NCBI36
NG_008051.1:g.26784A>T , LRG_583:g.26784A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1640A>T (F11) MANE Select	ENSP00000384957.2:p.Lys547Met
ENST00000264691.4:c.240A>T (F11)
ENST00000264692.8:c.1478A>T (F11)	ENSP00000264692.5:p.Lys493Met
ENST00000403665.6:c.1640A>T (F11)	ENSP00000384957.2:p.Lys547Met
ENST00000503841.1:n.159A>T (F11)
NM_000128.3:c.1640A>T , LRG_583t1:c.1640A>T (F11)	NP_000119.1:p.Lys547Met
NR_033900.1:n.1066+681T>A (F11-AS1)
XM_005262821.2:c.1643A>T (F11)	XP_005262878.1:p.Lys548Met
XM_005262822.2:c.1547A>T (F11)	XP_005262879.1:p.Lys516Met
XM_005262823.2:c.1373A>T (F11)	XP_005262880.1:p.Lys458Met
XM_006714137.1:c.1595A>T (F11)	XP_006714200.1:p.Lys532Met
XR_938707.1:n.1952A>T (F11)
XM_005262821.4:c.1643A>T (F11)	XP_005262878.1:p.Lys548Met
XM_005262822.4:c.1547A>T (F11)	XP_005262879.1:p.Lys516Met
XM_005262823.4:c.1373A>T (F11)	XP_005262880.1:p.Lys458Met
XM_006714137.3:c.1595A>T (F11)	XP_006714200.1:p.Lys532Met
NM_000128.4:c.1640A>T (F11) MANE Select	NP_000119.1:p.Lys547Met