Canonical Allele Identifier: CA358946395

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1359685833
• gnomAD v2: 4-187209761-C-T
• gnomAD v4: 4-186288607-C-T
• MyVariant Identifiers: chr4:g.187209761C>T (hg19) ; chr4:g.186288607C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288607C>T , CM000666.2:g.186288607C>T	GRCh38
NC_000004.11:g.187209761C>T , CM000666.1:g.187209761C>T	GRCh37
NC_000004.10:g.187446755C>T	NCBI36
NG_008051.1:g.27644C>T , LRG_583:g.27644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1871C>T (F11) MANE Select	ENSP00000384957.2:p.Ala624Val
ENST00000264691.4:c.471C>T (F11)
ENST00000264692.8:c.1709C>T (F11)	ENSP00000264692.5:p.Ala570Val
ENST00000403665.6:c.1871C>T (F11)	ENSP00000384957.2:p.Ala624Val
ENST00000503841.1:n.390C>T (F11)
NM_000128.3:c.1871C>T , LRG_583t1:c.1871C>T (F11)	NP_000119.1:p.Ala624Val
NR_033900.1:n.887G>A (F11-AS1)
XM_005262821.2:c.1874C>T (F11)	XP_005262878.1:p.Ala625Val
XM_005262822.2:c.1778C>T (F11)	XP_005262879.1:p.Ala593Val
XM_005262823.2:c.1604C>T (F11)	XP_005262880.1:p.Ala535Val
XM_006714137.1:c.1826C>T (F11)	XP_006714200.1:p.Ala609Val
XM_005262821.4:c.1874C>T (F11)	XP_005262878.1:p.Ala625Val
XM_005262822.4:c.1778C>T (F11)	XP_005262879.1:p.Ala593Val
XM_005262823.4:c.1604C>T (F11)	XP_005262880.1:p.Ala535Val
XM_006714137.3:c.1826C>T (F11)	XP_006714200.1:p.Ala609Val
NM_000128.4:c.1871C>T (F11) MANE Select	NP_000119.1:p.Ala624Val