Canonical Allele Identifier: CA358937819

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187201435T>G (hg19) ; chr4:g.186280281T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280281T>G , CM000666.2:g.186280281T>G	GRCh38
NC_000004.11:g.187201435T>G , CM000666.1:g.187201435T>G	GRCh37
NC_000004.10:g.187438429T>G	NCBI36
NG_008051.1:g.19318T>G , LRG_583:g.19318T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.924T>G MANE Select	ENSP00000384957.2:p.Ile308Met
ENST00000264692.8:c.762T>G	ENSP00000264692.5:p.Ile254Met
ENST00000403665.6:c.924T>G	ENSP00000384957.2:p.Ile308Met
ENST00000452239.1:c.371T>G
NM_000128.3:c.924T>G , LRG_583t1:c.924T>G	NP_000119.1:p.Ile308Met
XM_005262821.2:c.924T>G	XP_005262878.1:p.Ile308Met
XM_005262822.2:c.924T>G	XP_005262879.1:p.Ile308Met
XM_005262823.2:c.654T>G	XP_005262880.1:p.Ile218Met
XM_005262824.1:c.924T>G	XP_005262881.1:p.Ile308Met
XM_006714137.1:c.876T>G	XP_006714200.1:p.Ile292Met
XR_938706.1:n.1276T>G
XR_938707.1:n.1276T>G
XM_005262821.4:c.924T>G	XP_005262878.1:p.Ile308Met
XM_005262822.4:c.924T>G	XP_005262879.1:p.Ile308Met
XM_005262823.4:c.654T>G	XP_005262880.1:p.Ile218Met
XM_006714137.3:c.876T>G	XP_006714200.1:p.Ile292Met
XM_017007884.2:c.924T>G	XP_016863373.1:p.Ile308Met
XM_017007885.2:c.924T>G	XP_016863374.1:p.Ile308Met
XM_017007886.2:c.924T>G	XP_016863375.1:p.Ile308Met
XR_001741172.2:n.1257T>G
NM_000128.4:c.924T>G MANE Select	NP_000119.1:p.Ile308Met