Canonical Allele Identifier: CA358942316

Gene: F11

Linked Data

• gnomAD v4: 4-186284255-C-A
• MyVariant Identifiers: chr4:g.187205409C>A (hg19) ; chr4:g.186284255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284255C>A , CM000666.2:g.186284255C>A	GRCh38
NC_000004.11:g.187205409C>A , CM000666.1:g.187205409C>A	GRCh37
NC_000004.10:g.187442403C>A	NCBI36
NG_008051.1:g.23292C>A , LRG_583:g.23292C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1299C>A MANE Select	ENSP00000384957.2:p.Phe433Leu
ENST00000264692.8:c.1137C>A	ENSP00000264692.5:p.Phe379Leu
ENST00000403665.6:c.1299C>A	ENSP00000384957.2:p.Phe433Leu
NM_000128.3:c.1299C>A , LRG_583t1:c.1299C>A	NP_000119.1:p.Phe433Leu
XM_005262821.2:c.1302C>A	XP_005262878.1:p.Phe434Leu
XM_005262822.2:c.1302C>A	XP_005262879.1:p.Phe434Leu
XM_005262823.2:c.1032C>A	XP_005262880.1:p.Phe344Leu
XM_005262824.1:c.1302C>A	XP_005262881.1:p.Phe434Leu
XM_006714137.1:c.1254C>A	XP_006714200.1:p.Phe418Leu
XR_938706.1:n.1707C>A
XR_938707.1:n.1707C>A
XM_005262821.4:c.1302C>A	XP_005262878.1:p.Phe434Leu
XM_005262822.4:c.1302C>A	XP_005262879.1:p.Phe434Leu
XM_005262823.4:c.1032C>A	XP_005262880.1:p.Phe344Leu
XM_006714137.3:c.1254C>A	XP_006714200.1:p.Phe418Leu
XR_001741172.2:n.1773C>A
NM_000128.4:c.1299C>A MANE Select	NP_000119.1:p.Phe433Leu