Canonical Allele Identifier: CA442641038

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187207615A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286461A>T , CM000666.2:g.186286461A>T	GRCh38
NC_000004.11:g.187207615A>T , CM000666.1:g.187207615A>T	GRCh37
NC_000004.10:g.187444609A>T	NCBI36
NG_008051.1:g.25498A>T , LRG_583:g.25498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1527A>T (F11) MANE Select	ENSP00000384957.2:p.Val509=
ENST00000264691.4:c.176+648A>T (F11)
ENST00000264692.8:c.1365A>T (F11)	ENSP00000264692.5:p.Val455=
ENST00000403665.6:c.1527A>T (F11)	ENSP00000384957.2:p.Val509=
NM_000128.3:c.1527A>T , LRG_583t1:c.1527A>T (F11)	NP_000119.1:p.Val509=
NR_033900.1:n.1067-195T>A (F11-AS1)
XM_005262821.2:c.1530A>T (F11)	XP_005262878.1:p.Val510=
XM_005262822.2:c.1483+648A>T (F11)	XP_005262879.1:n.1483+648A>T
XM_005262823.2:c.1260A>T (F11)	XP_005262880.1:p.Val420=
XM_005262824.1:c.1484-85A>T (F11)	XP_005262881.1:n.1484-85A>T
XM_006714137.1:c.1482A>T (F11)	XP_006714200.1:p.Val494=
XR_938706.1:n.1935A>T (F11)
XR_938707.1:n.1888+648A>T (F11)
XM_005262821.4:c.1530A>T (F11)	XP_005262878.1:p.Val510=
XM_005262822.4:c.1483+648A>T (F11)	XP_005262879.1:n.1483+648A>T
XM_005262823.4:c.1260A>T (F11)	XP_005262880.1:p.Val420=
XM_006714137.3:c.1482A>T (F11)	XP_006714200.1:p.Val494=
XR_001741172.2:n.2001A>T (F11)
NM_000128.4:c.1527A>T (F11) MANE Select	NP_000119.1:p.Val509=