Canonical Allele Identifier: CA358941718

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205293G>A (hg19) ; chr4:g.186284139G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284139G>A , CM000666.2:g.186284139G>A	GRCh38
NC_000004.11:g.187205293G>A , CM000666.1:g.187205293G>A	GRCh37
NC_000004.10:g.187442287G>A	NCBI36
NG_008051.1:g.23176G>A , LRG_583:g.23176G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1183G>A MANE Select	ENSP00000384957.2:p.Val395Ile
ENST00000264692.8:c.1021G>A	ENSP00000264692.5:p.Val341Ile
ENST00000403665.6:c.1183G>A	ENSP00000384957.2:p.Val395Ile
NM_000128.3:c.1183G>A , LRG_583t1:c.1183G>A	NP_000119.1:p.Val395Ile
XM_005262821.2:c.1186G>A	XP_005262878.1:p.Val396Ile
XM_005262822.2:c.1186G>A	XP_005262879.1:p.Val396Ile
XM_005262823.2:c.916G>A	XP_005262880.1:p.Val306Ile
XM_005262824.1:c.1186G>A	XP_005262881.1:p.Val396Ile
XM_006714137.1:c.1138G>A	XP_006714200.1:p.Val380Ile
XR_938706.1:n.1591G>A
XR_938707.1:n.1591G>A
XM_005262821.4:c.1186G>A	XP_005262878.1:p.Val396Ile
XM_005262822.4:c.1186G>A	XP_005262879.1:p.Val396Ile
XM_005262823.4:c.916G>A	XP_005262880.1:p.Val306Ile
XM_006714137.3:c.1138G>A	XP_006714200.1:p.Val380Ile
XM_017007884.2:c.*2155G>A	XP_016863373.1:n.*2155G>A
XM_017007885.2:c.*51G>A	XP_016863374.1:n.*51G>A
XR_001741172.2:n.1657G>A
NM_000128.4:c.1183G>A MANE Select	NP_000119.1:p.Val395Ile