Canonical Allele Identifier: CA358946197

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209696G>T (hg19) ; chr4:g.186288542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288542G>T , CM000666.2:g.186288542G>T	GRCh38
NC_000004.11:g.187209696G>T , CM000666.1:g.187209696G>T	GRCh37
NC_000004.10:g.187446690G>T	NCBI36
NG_008051.1:g.27579G>T , LRG_583:g.27579G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1806G>T (F11) MANE Select	ENSP00000384957.2:p.Arg602Ser
ENST00000264691.4:c.406G>T (F11)
ENST00000264692.8:c.1644G>T (F11)	ENSP00000264692.5:p.Arg548Ser
ENST00000403665.6:c.1806G>T (F11)	ENSP00000384957.2:p.Arg602Ser
ENST00000503841.1:n.325G>T (F11)
NM_000128.3:c.1806G>T , LRG_583t1:c.1806G>T (F11)	NP_000119.1:p.Arg602Ser
NR_033900.1:n.952C>A (F11-AS1)
XM_005262821.2:c.1809G>T (F11)	XP_005262878.1:p.Arg603Ser
XM_005262822.2:c.1713G>T (F11)	XP_005262879.1:p.Arg571Ser
XM_005262823.2:c.1539G>T (F11)	XP_005262880.1:p.Arg513Ser
XM_006714137.1:c.1761G>T (F11)	XP_006714200.1:p.Arg587Ser
XM_005262821.4:c.1809G>T (F11)	XP_005262878.1:p.Arg603Ser
XM_005262822.4:c.1713G>T (F11)	XP_005262879.1:p.Arg571Ser
XM_005262823.4:c.1539G>T (F11)	XP_005262880.1:p.Arg513Ser
XM_006714137.3:c.1761G>T (F11)	XP_006714200.1:p.Arg587Ser
NM_000128.4:c.1806G>T (F11) MANE Select	NP_000119.1:p.Arg602Ser