Canonical Allele Identifier: CA3164127

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs758171404
• ExAC: 4:187209696 G / A
• gnomAD v2: 4-187209696-G-A
• gnomAD v3: 4-186288542-G-A
• gnomAD v4: 4-186288542-G-A
• MyVariant Identifiers: chr4:g.187209696G>A (hg19) ; chr4:g.186288542G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1806G>A (F11) MANE Select	ENSP00000384957.2:p.Arg602=
ENST00000264691.4:c.406G>A (F11)
ENST00000264692.8:c.1644G>A (F11)	ENSP00000264692.5:p.Arg548=
ENST00000403665.6:c.1806G>A (F11)	ENSP00000384957.2:p.Arg602=
ENST00000503841.1:n.325G>A (F11)
NM_000128.3:c.1806G>A , LRG_583t1:c.1806G>A (F11)	NP_000119.1:p.Arg602=
NR_033900.1:n.952C>T (F11-AS1)
XM_005262821.2:c.1809G>A (F11)	XP_005262878.1:p.Arg603=
XM_005262822.2:c.1713G>A (F11)	XP_005262879.1:p.Arg571=
XM_005262823.2:c.1539G>A (F11)	XP_005262880.1:p.Arg513=
XM_006714137.1:c.1761G>A (F11)	XP_006714200.1:p.Arg587=
XM_005262821.4:c.1809G>A (F11)	XP_005262878.1:p.Arg603=
XM_005262822.4:c.1713G>A (F11)	XP_005262879.1:p.Arg571=
XM_005262823.4:c.1539G>A (F11)	XP_005262880.1:p.Arg513=
XM_006714137.3:c.1761G>A (F11)	XP_006714200.1:p.Arg587=
NM_000128.4:c.1806G>A (F11) MANE Select	NP_000119.1:p.Arg602=