Canonical Allele Identifier: CA3163733

Gene: F11

Linked Data

• ClinVar Variation Id: 1676750
• ClinVar RCV Id: RCV002222147
• dbSNP Id: rs779123395
• ExAC: 4:187197405 C / T
• gnomAD v2: 4-187197405-C-T
• gnomAD v3: 4-186276251-C-T
• gnomAD v4: 4-186276251-C-T
• MyVariant Identifiers: chr4:g.187197405C>T (hg19) ; chr4:g.186276251C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276251C>T , CM000666.2:g.186276251C>T	GRCh38
NC_000004.11:g.187197405C>T , CM000666.1:g.187197405C>T	GRCh37
NC_000004.10:g.187434399C>T	NCBI36
NG_008051.1:g.15288C>T , LRG_583:g.15288C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.616C>T MANE Select	ENSP00000384957.2:p.Pro206Ser
ENST00000264692.8:c.454C>T	ENSP00000264692.5:p.Pro152Ser
ENST00000403665.6:c.616C>T	ENSP00000384957.2:p.Pro206Ser
ENST00000452239.1:c.63C>T
NM_000128.3:c.616C>T , LRG_583t1:c.616C>T	NP_000119.1:p.Pro206Ser
XM_005262821.2:c.616C>T	XP_005262878.1:p.Pro206Ser
XM_005262822.2:c.616C>T	XP_005262879.1:p.Pro206Ser
XM_005262823.2:c.485+1976C>T	XP_005262880.1:n.485+1976C>T
XM_005262824.1:c.616C>T	XP_005262881.1:p.Pro206Ser
XM_006714137.1:c.616C>T	XP_006714200.1:p.Pro206Ser
XR_938706.1:n.968C>T
XR_938707.1:n.968C>T
XM_005262821.4:c.616C>T	XP_005262878.1:p.Pro206Ser
XM_005262822.4:c.616C>T	XP_005262879.1:p.Pro206Ser
XM_005262823.4:c.485+1976C>T	XP_005262880.1:n.485+1976C>T
XM_006714137.3:c.616C>T	XP_006714200.1:p.Pro206Ser
XM_017007884.2:c.616C>T	XP_016863373.1:p.Pro206Ser
XM_017007885.2:c.616C>T	XP_016863374.1:p.Pro206Ser
XM_017007886.2:c.616C>T	XP_016863375.1:p.Pro206Ser
XR_001741172.2:n.949C>T
NM_000128.4:c.616C>T MANE Select	NP_000119.1:p.Pro206Ser