Canonical Allele Identifier: CA442640176

Gene: F11

Linked Data

• dbSNP Id: rs1192339570
• gnomAD v2: 4-187206933-C-G
• gnomAD v4: 4-186285779-C-G
• MyVariant Identifiers: chr4:g.187206933C>G (hg19) ; chr4:g.186285779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285779C>G , CM000666.2:g.186285779C>G	GRCh38
NC_000004.11:g.187206933C>G , CM000666.1:g.187206933C>G	GRCh37
NC_000004.10:g.187443927C>G	NCBI36
NG_008051.1:g.24816C>G , LRG_583:g.24816C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1446C>G MANE Select	ENSP00000384957.2:p.Ala482=
ENST00000264691.4:c.142C>G
ENST00000264692.8:c.1284C>G	ENSP00000264692.5:p.Ala428=
ENST00000403665.6:c.1446C>G	ENSP00000384957.2:p.Ala482=
NM_000128.3:c.1446C>G , LRG_583t1:c.1446C>G	NP_000119.1:p.Ala482=
XM_005262821.2:c.1449C>G	XP_005262878.1:p.Ala483=
XM_005262822.2:c.1449C>G	XP_005262879.1:p.Ala483=
XM_005262823.2:c.1179C>G	XP_005262880.1:p.Ala393=
XM_005262824.1:c.1449C>G	XP_005262881.1:p.Ala483=
XM_006714137.1:c.1401C>G	XP_006714200.1:p.Ala467=
XR_938706.1:n.1854C>G
XR_938707.1:n.1854C>G
XM_005262821.4:c.1449C>G	XP_005262878.1:p.Ala483=
XM_005262822.4:c.1449C>G	XP_005262879.1:p.Ala483=
XM_005262823.4:c.1179C>G	XP_005262880.1:p.Ala393=
XM_006714137.3:c.1401C>G	XP_006714200.1:p.Ala467=
XR_001741172.2:n.1920C>G
NM_000128.4:c.1446C>G MANE Select	NP_000119.1:p.Ala482=