Canonical Allele Identifier: CA3163795

Gene: F11

Linked Data

• ClinVar Variation Id: 989864
• ClinVar RCV Id: RCV001277766
• dbSNP Id: rs745814397
• ExAC: 4:187201262 G / C
• gnomAD v2: 4-187201262-G-C
• gnomAD v3: 4-186280108-G-C
• gnomAD v4: 4-186280108-G-C
• MyVariant Identifiers: chr4:g.187201262G>C (hg19) ; chr4:g.186280108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280108G>C , CM000666.2:g.186280108G>C	GRCh38
NC_000004.11:g.187201262G>C , CM000666.1:g.187201262G>C	GRCh37
NC_000004.10:g.187438256G>C	NCBI36
NG_008051.1:g.19145G>C , LRG_583:g.19145G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.852G>C MANE Select	ENSP00000384957.2:p.Arg284Ser
ENST00000264692.8:c.690G>C	ENSP00000264692.5:p.Arg230Ser
ENST00000403665.6:c.852G>C	ENSP00000384957.2:p.Arg284Ser
ENST00000452239.1:c.299G>C
NM_000128.3:c.852G>C , LRG_583t1:c.852G>C	NP_000119.1:p.Arg284Ser
XM_005262821.2:c.852G>C	XP_005262878.1:p.Arg284Ser
XM_005262822.2:c.852G>C	XP_005262879.1:p.Arg284Ser
XM_005262823.2:c.582G>C	XP_005262880.1:p.Arg194Ser
XM_005262824.1:c.852G>C	XP_005262881.1:p.Arg284Ser
XM_006714137.1:c.852G>C	XP_006714200.1:p.Arg284Ser
XR_938706.1:n.1204G>C
XR_938707.1:n.1204G>C
XM_005262821.4:c.852G>C	XP_005262878.1:p.Arg284Ser
XM_005262822.4:c.852G>C	XP_005262879.1:p.Arg284Ser
XM_005262823.4:c.582G>C	XP_005262880.1:p.Arg194Ser
XM_006714137.3:c.852G>C	XP_006714200.1:p.Arg284Ser
XM_017007884.2:c.852G>C	XP_016863373.1:p.Arg284Ser
XM_017007885.2:c.852G>C	XP_016863374.1:p.Arg284Ser
XM_017007886.2:c.852G>C	XP_016863375.1:p.Arg284Ser
XR_001741172.2:n.1185G>C
NM_000128.4:c.852G>C MANE Select	NP_000119.1:p.Arg284Ser