Canonical Allele Identifier: CA358946102

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741383300
• MyVariant Identifiers: chr4:g.187209676G>T (hg19) ; chr4:g.186288522G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288522G>T , CM000666.2:g.186288522G>T	GRCh38
NC_000004.11:g.187209676G>T , CM000666.1:g.187209676G>T	GRCh37
NC_000004.10:g.187446670G>T	NCBI36
NG_008051.1:g.27559G>T , LRG_583:g.27559G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1786G>T (F11) MANE Select	ENSP00000384957.2:p.Gly596Cys
ENST00000264691.4:c.386G>T (F11)
ENST00000264692.8:c.1624G>T (F11)	ENSP00000264692.5:p.Gly542Cys
ENST00000403665.6:c.1786G>T (F11)	ENSP00000384957.2:p.Gly596Cys
ENST00000503841.1:n.305G>T (F11)
NM_000128.3:c.1786G>T , LRG_583t1:c.1786G>T (F11)	NP_000119.1:p.Gly596Cys
NR_033900.1:n.972C>A (F11-AS1)
XM_005262821.2:c.1789G>T (F11)	XP_005262878.1:p.Gly597Cys
XM_005262822.2:c.1693G>T (F11)	XP_005262879.1:p.Gly565Cys
XM_005262823.2:c.1519G>T (F11)	XP_005262880.1:p.Gly507Cys
XM_006714137.1:c.1741G>T (F11)	XP_006714200.1:p.Gly581Cys
XM_005262821.4:c.1789G>T (F11)	XP_005262878.1:p.Gly597Cys
XM_005262822.4:c.1693G>T (F11)	XP_005262879.1:p.Gly565Cys
XM_005262823.4:c.1519G>T (F11)	XP_005262880.1:p.Gly507Cys
XM_006714137.3:c.1741G>T (F11)	XP_006714200.1:p.Gly581Cys
NM_000128.4:c.1786G>T (F11) MANE Select	NP_000119.1:p.Gly596Cys