Canonical Allele Identifier: CA358945516

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs774280710
• gnomAD v2: 4-187208869-G-T
• gnomAD v4: 4-186287715-G-T
• MyVariant Identifiers: chr4:g.187208869G>T (hg19) ; chr4:g.186287715G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287715G>T , CM000666.2:g.186287715G>T	GRCh38
NC_000004.11:g.187208869G>T , CM000666.1:g.187208869G>T	GRCh37
NC_000004.10:g.187445863G>T	NCBI36
NG_008051.1:g.26752G>T , LRG_583:g.26752G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1608G>T (F11) MANE Select	ENSP00000384957.2:p.Lys536Asn
ENST00000264691.4:c.208G>T (F11)
ENST00000264692.8:c.1446G>T (F11)	ENSP00000264692.5:p.Lys482Asn
ENST00000403665.6:c.1608G>T (F11)	ENSP00000384957.2:p.Lys536Asn
ENST00000503841.1:n.127G>T (F11)
NM_000128.3:c.1608G>T , LRG_583t1:c.1608G>T (F11)	NP_000119.1:p.Lys536Asn
NR_033900.1:n.1066+713C>A (F11-AS1)
XM_005262821.2:c.1611G>T (F11)	XP_005262878.1:p.Lys537Asn
XM_005262822.2:c.1515G>T (F11)	XP_005262879.1:p.Lys505Asn
XM_005262823.2:c.1341G>T (F11)	XP_005262880.1:p.Lys447Asn
XM_006714137.1:c.1563G>T (F11)	XP_006714200.1:p.Lys521Asn
XR_938707.1:n.1920G>T (F11)
XM_005262821.4:c.1611G>T (F11)	XP_005262878.1:p.Lys537Asn
XM_005262822.4:c.1515G>T (F11)	XP_005262879.1:p.Lys505Asn
XM_005262823.4:c.1341G>T (F11)	XP_005262880.1:p.Lys447Asn
XM_006714137.3:c.1563G>T (F11)	XP_006714200.1:p.Lys521Asn
NM_000128.4:c.1608G>T (F11) MANE Select	NP_000119.1:p.Lys536Asn