Canonical Allele Identifier: CA442638962

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205295T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284141T>C , CM000666.2:g.186284141T>C	GRCh38
NC_000004.11:g.187205295T>C , CM000666.1:g.187205295T>C	GRCh37
NC_000004.10:g.187442289T>C	NCBI36
NG_008051.1:g.23178T>C , LRG_583:g.23178T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1185T>C MANE Select	ENSP00000384957.2:p.Val395=
ENST00000264692.8:c.1023T>C	ENSP00000264692.5:p.Val341=
ENST00000403665.6:c.1185T>C	ENSP00000384957.2:p.Val395=
NM_000128.3:c.1185T>C , LRG_583t1:c.1185T>C	NP_000119.1:p.Val395=
XM_005262821.2:c.1188T>C	XP_005262878.1:p.Val396=
XM_005262822.2:c.1188T>C	XP_005262879.1:p.Val396=
XM_005262823.2:c.918T>C	XP_005262880.1:p.Val306=
XM_005262824.1:c.1188T>C	XP_005262881.1:p.Val396=
XM_006714137.1:c.1140T>C	XP_006714200.1:p.Val380=
XR_938706.1:n.1593T>C
XR_938707.1:n.1593T>C
XM_005262821.4:c.1188T>C	XP_005262878.1:p.Val396=
XM_005262822.4:c.1188T>C	XP_005262879.1:p.Val396=
XM_005262823.4:c.918T>C	XP_005262880.1:p.Val306=
XM_006714137.3:c.1140T>C	XP_006714200.1:p.Val380=
XM_017007884.2:c.*2157T>C	XP_016863373.1:n.*2157T>C
XM_017007885.2:c.*53T>C	XP_016863374.1:n.*53T>C
XR_001741172.2:n.1659T>C
NM_000128.4:c.1185T>C MANE Select	NP_000119.1:p.Val395=