Canonical Allele Identifier: CA442644072

Gene: F11

Linked Data

• ClinVar Variation Id: 1532179
• ClinVar RCV Id: RCV002102005
• dbSNP Id: rs1328599983
• gnomAD v4: 4-186271652-G-A
• MyVariant Identifiers: chr4:g.187192806G>A (hg19) ; chr4:g.186271652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186271652G>A , CM000666.2:g.186271652G>A	GRCh38
NC_000004.11:g.187192806G>A , CM000666.1:g.187192806G>A	GRCh37
NC_000004.10:g.187429800G>A	NCBI36
NG_008051.1:g.10689G>A , LRG_583:g.10689G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.99G>A MANE Select	ENSP00000384957.2:p.Gly33=
ENST00000264692.8:c.99G>A	ENSP00000264692.5:p.Gly33=
ENST00000403665.6:c.99G>A	ENSP00000384957.2:p.Gly33=
ENST00000492972.6:c.99G>A	ENSP00000424479.1:p.Gly33=
NM_000128.3:c.99G>A , LRG_583t1:c.99G>A	NP_000119.1:p.Gly33=
XM_005262821.2:c.99G>A	XP_005262878.1:p.Gly33=
XM_005262822.2:c.99G>A	XP_005262879.1:p.Gly33=
XM_005262823.2:c.99G>A	XP_005262880.1:p.Gly33=
XM_005262824.1:c.99G>A	XP_005262881.1:p.Gly33=
XM_006714137.1:c.99G>A	XP_006714200.1:p.Gly33=
XR_938706.1:n.451G>A
XR_938707.1:n.451G>A
NM_001354804.1:c.99G>A	NP_001341733.1:p.Gly33=
XM_005262821.4:c.99G>A	XP_005262878.1:p.Gly33=
XM_005262822.4:c.99G>A	XP_005262879.1:p.Gly33=
XM_005262823.4:c.99G>A	XP_005262880.1:p.Gly33=
XM_006714137.3:c.99G>A	XP_006714200.1:p.Gly33=
XM_017007884.2:c.99G>A	XP_016863373.1:p.Gly33=
XM_017007885.2:c.99G>A	XP_016863374.1:p.Gly33=
XM_017007886.2:c.99G>A	XP_016863375.1:p.Gly33=
XR_001741172.2:n.432G>A
NM_000128.4:c.99G>A MANE Select	NP_000119.1:p.Gly33=
NM_001354804.2:c.99G>A	NP_001341733.1:p.Gly33=