Canonical Allele Identifier: CA358943531

Gene: F11

Linked Data

• gnomAD v4: 4-186285760-A-G
• MyVariant Identifiers: chr4:g.187206914A>G (hg19) ; chr4:g.186285760A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285760A>G , CM000666.2:g.186285760A>G	GRCh38
NC_000004.11:g.187206914A>G , CM000666.1:g.187206914A>G	GRCh37
NC_000004.10:g.187443908A>G	NCBI36
NG_008051.1:g.24797A>G , LRG_583:g.24797A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1427A>G MANE Select	ENSP00000384957.2:p.Glu476Gly
ENST00000264691.4:c.123A>G
ENST00000264692.8:c.1265A>G	ENSP00000264692.5:p.Glu422Gly
ENST00000403665.6:c.1427A>G	ENSP00000384957.2:p.Glu476Gly
NM_000128.3:c.1427A>G , LRG_583t1:c.1427A>G	NP_000119.1:p.Glu476Gly
XM_005262821.2:c.1430A>G	XP_005262878.1:p.Glu477Gly
XM_005262822.2:c.1430A>G	XP_005262879.1:p.Glu477Gly
XM_005262823.2:c.1160A>G	XP_005262880.1:p.Glu387Gly
XM_005262824.1:c.1430A>G	XP_005262881.1:p.Glu477Gly
XM_006714137.1:c.1382A>G	XP_006714200.1:p.Glu461Gly
XR_938706.1:n.1835A>G
XR_938707.1:n.1835A>G
XM_005262821.4:c.1430A>G	XP_005262878.1:p.Glu477Gly
XM_005262822.4:c.1430A>G	XP_005262879.1:p.Glu477Gly
XM_005262823.4:c.1160A>G	XP_005262880.1:p.Glu387Gly
XM_006714137.3:c.1382A>G	XP_006714200.1:p.Glu461Gly
XR_001741172.2:n.1901A>G
NM_000128.4:c.1427A>G MANE Select	NP_000119.1:p.Glu476Gly