Canonical Allele Identifier: CA358938092

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187201479A>T (hg19) ; chr4:g.186280325A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280325A>T , CM000666.2:g.186280325A>T	GRCh38
NC_000004.11:g.187201479A>T , CM000666.1:g.187201479A>T	GRCh37
NC_000004.10:g.187438473A>T	NCBI36
NG_008051.1:g.19362A>T , LRG_583:g.19362A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.968A>T MANE Select	ENSP00000384957.2:p.Asn323Ile
ENST00000264692.8:c.806A>T	ENSP00000264692.5:p.Asn269Ile
ENST00000403665.6:c.968A>T	ENSP00000384957.2:p.Asn323Ile
ENST00000452239.1:c.415A>T
NM_000128.3:c.968A>T , LRG_583t1:c.968A>T	NP_000119.1:p.Asn323Ile
XM_005262821.2:c.968A>T	XP_005262878.1:p.Asn323Ile
XM_005262822.2:c.968A>T	XP_005262879.1:p.Asn323Ile
XM_005262823.2:c.698A>T	XP_005262880.1:p.Asn233Ile
XM_005262824.1:c.968A>T	XP_005262881.1:p.Asn323Ile
XM_006714137.1:c.920A>T	XP_006714200.1:p.Asn307Ile
XR_938706.1:n.1320A>T
XR_938707.1:n.1320A>T
XM_005262821.4:c.968A>T	XP_005262878.1:p.Asn323Ile
XM_005262822.4:c.968A>T	XP_005262879.1:p.Asn323Ile
XM_005262823.4:c.698A>T	XP_005262880.1:p.Asn233Ile
XM_006714137.3:c.920A>T	XP_006714200.1:p.Asn307Ile
XM_017007884.2:c.968A>T	XP_016863373.1:p.Asn323Ile
XM_017007885.2:c.968A>T	XP_016863374.1:p.Asn323Ile
XM_017007886.2:c.968A>T	XP_016863375.1:p.Asn323Ile
XR_001741172.2:n.1301A>T
NM_000128.4:c.968A>T MANE Select	NP_000119.1:p.Asn323Ile