Canonical Allele Identifier: CA442641297

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs374968287
• gnomAD v2: 4-187209592-C-T
• gnomAD v4: 4-186288438-C-T
• MyVariant Identifiers: chr4:g.187209592C>T (hg19) ; chr4:g.186288438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288438C>T , CM000666.2:g.186288438C>T	GRCh38
NC_000004.11:g.187209592C>T , CM000666.1:g.187209592C>T	GRCh37
NC_000004.10:g.187446586C>T	NCBI36
NG_008051.1:g.27475C>T , LRG_583:g.27475C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1717-15C>T (F11) MANE Select	ENSP00000384957.2:n.1717-15C>T
ENST00000264691.4:c.317-15C>T (F11)
ENST00000264692.8:c.1555-15C>T (F11)	ENSP00000264692.5:n.1555-15C>T
ENST00000403665.6:c.1717-15C>T (F11)	ENSP00000384957.2:n.1717-15C>T
ENST00000503841.1:n.236-15C>T (F11)
NM_000128.3:c.1717-15C>T , LRG_583t1:c.1717-15C>T (F11)	NP_000119.1:n.1717-15C>T
NR_033900.1:n.1056G>A (F11-AS1)
XM_005262821.2:c.1720-15C>T (F11)	XP_005262878.1:n.1720-15C>T
XM_005262822.2:c.1624-15C>T (F11)	XP_005262879.1:n.1624-15C>T
XM_005262823.2:c.1450-15C>T (F11)	XP_005262880.1:n.1450-15C>T
XM_006714137.1:c.1672-15C>T (F11)	XP_006714200.1:n.1672-15C>T
XM_005262821.4:c.1720-15C>T (F11)	XP_005262878.1:n.1720-15C>T
XM_005262822.4:c.1624-15C>T (F11)	XP_005262879.1:n.1624-15C>T
XM_005262823.4:c.1450-15C>T (F11)	XP_005262880.1:n.1450-15C>T
XM_006714137.3:c.1672-15C>T (F11)	XP_006714200.1:n.1672-15C>T
NM_000128.4:c.1717-15C>T (F11) MANE Select	NP_000119.1:n.1717-15C>T